O-Shot Consent Template

Key Takeaways

O-Shot consent forms must document PRP origin, risks, contraindications, and patient understanding

Separate absolute and relative contraindications for clinical accuracy and screening efficiency

Include tiered risk disclosures covering infection, bruising, temporary dysesthesia, and rare complications

Digital signature workflows streamline pre-appointment completion and CQC compliance

Customisable templates save clinic time while maintaining medico-legal protection

The o-shot consent form is a critical legal and clinical document for aesthetic clinics offering Orgasm Shot treatments. This procedure uses platelet-rich plasma (PRP) derived from the patient’s own blood to enhance intimate health and sexual wellness in women-and your consent documentation must reflect both the benefits and the real risks involved.

A comprehensive o-shot consent form does more than satisfy regulatory requirements. It demonstrates informed consent, protects your clinic from liability, and ensures patients genuinely understand the procedure before treatment. This guide explains what a professional O-Shot consent form must contain, how to implement it into your pre-appointment workflow, and how to adapt a template to your clinic’s specific protocols and patient population.

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O-Shot Consent Form

A ready-to-use consent form template covering patient details, contraindication screening (absolute and relative tiers), risk disclosures for PRP injection, expected outcomes, anesthesia administration, alternative treatments, post-procedure care instructions, and digital signature blocks for compliance.

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What is an O-Shot Consent Form?

An O-Shot consent form is a medical-legal document designed specifically for aesthetic clinics performing Orgasm Shot (PRP) procedures on the clitoris and vaginal tissue. It serves three critical functions: documenting that the patient understands the procedure, acknowledging the associated risks, and establishing informed consent under UK law (CQC and GMC standards).

The O-Shot uses autologous platelet-rich plasma clinical research-platelets extracted from the patient’s own blood-injected into targeted areas of the clitoris and anterior vaginal wall. While limited scientific evidence supporting O-Shot exists, clinics must ensure consent forms address this uncertainty. Unlike standardised cosmetic procedures, the O-Shot sits at the intersection of aesthetic medicine and sexual wellness therapy. Your consent form must address both clinical safety and patient expectations around intimate outcomes.

A professional consent form covers procedure description, contraindications (absolute conditions that prevent treatment, and relative conditions requiring clinician judgement), documented risks ranging from common to rare, expected timelines for results, alternatives to PRP, anesthesia methods, and post-procedure care. It also includes sections for patient acknowledgment and signature-increasingly digital signatures for paperless, GDPR-compliant workflows.

How to Use the O-Shot Consent Form

Implement the o-shot consent form into your clinic workflow using these five operational steps. Ensure your compliance management workflow aligns with your medical director’s protocols before customising the form.

1. Tailor contraindication screening to your patient base. Review absolute contraindications (conditions that exclude all O-Shot candidates) and relative contraindications (conditions requiring clinical assessment). Absolute contraindications typically include active infection, pregnancy, anticoagulation therapy, and certain bleeding disorders. Relative contraindications include recent injectable fillers, vaginal procedure history within 3 months, and specific dermatological conditions. Adjust the list to reflect your medical director’s protocols.
2. Customise procedure description and timeline. Insert your clinic’s specific O-Shot protocol: injection sites, PRP processing method, numbing approach, and expected treatment duration. Include realistic timelines-results typically appear over 3-6 weeks as PRP-derived growth factors initiate tissue remodelling, with peak outcomes at 3 months. Your consent form should also disclose that the O-Shot is not FDA-approved despite its documented use across multiple fields.
3. Document risk tiers clearly. Structure risk disclosure as common (expected, self-limiting) and rare (requiring immediate care). Common risks include bruising, swelling, temporary discomfort, and mild dysesthesia. Rare risks include infection, hematoma, prolonged dysesthesia, and unsatisfactory results. Specify your clinic’s post-care infection prevention protocol and red flags requiring immediate contact. Ensure your medical team follows trained O-Shot provider protocols for blood processing and sterile injection techniques.
4. Include alternative treatment options. State alternatives to O-Shot PRP: observation, topical oestrogen or vaginal moisturisers, pelvic floor physiotherapy, or referral to sexual health specialists. This demonstrates informed choice and strengthens consent validity.
5. Integrate digital signature and pre-appointment completion. Deploy the form through your clinic’s digital forms platform at least 48 hours before treatment. Digital signatures create audit trails, reduce paperwork, and ensure GDPR compliance. Have patients complete the form before arrival; clinic staff review for completeness.

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Who is the O-Shot Consent Form Helpful For?

The o-shot consent form is essential for several practice types. Aesthetic and medical spas offering PRP vaginal rejuvenation benefit from procedure-specific documentation that clarifies what O-Shot can and cannot achieve, reducing post-treatment dissatisfaction across diverse patient populations.

Private gynaecology and sexual health clinics integrating regenerative medicine, particularly Cellular Medicine Association certified providers, can adapt the form can adapt the form to their patient communication style while maintaining rigorous risk disclosure standards. Dermatology and aesthetic medicine practices expanding into intimate area treatments gain a bridge between clinical training and sexual wellness terminology.

Multi-location aesthetic groups and franchises need standardised documentation across locations-a template ensures every clinic meets CQC standards and medico-legal requirements while allowing local customisation. Independent practitioner-led clinics without dedicated compliance staff accelerate setup by adapting a ready-made template, reducing legal review time and preventing critical omissions.

Benefits of Using an O-Shot Consent Form Template

Medico-legal protection: A detailed, signed consent form demonstrates informed decision-making under UK law (GMC and CQC standards). If a patient claims they didn’t understand risks or were unaware of alternatives, your documentation provides evidence of thorough disclosure. This is particularly important for intimate procedures where patient expectations and outcomes can diverge significantly.

Compliance with regulatory bodies: The Care Quality Commission (CQC) inspects consent practices during aesthetic clinic assessments. A procedure-specific form with tiered risk disclosure and contraindication screening signals robust governance. Use digital forms platforms to streamline signature collection while maintaining audit trails.

Reduced post-treatment disputes: Clear documentation of expected outcomes and realistic timelines prevents patients from claiming they were promised immediate results. Stating alternatives acknowledges that O-Shot is one option, not the only solution-managing expectations upfront.

Faster clinic onboarding: A template accelerates consent process design for new clinics or practitioners. Rather than starting from scratch, you inherit a procedure-specific framework tested across hundreds of clinics. New team members understand what questions matter, why contraindication screening is tiered, and what post-care information is critical.

Risk Disclosure and Patient Safety in O-Shot Procedures

Risk disclosure is the ethical and legal cornerstone of informed consent. For O-Shot procedures, risks are tiered-common, self-limiting risks that nearly all patients experience briefly, and rare but serious risks that require immediate attention.

Common risks include bruising (resolves in 7-14 days), swelling of the injection sites (peaks at 24-48 hours, subsides over 1 week), temporary discomfort or aching, and mild dysesthesia or altered sensation (typically resolves within 2 weeks). These are expected outcomes of PRP injection into sensitive tissue. Your consent form should frame them as transient, normal responses-not complications.

Rare but serious risks require explicit documentation. Infection is the most concerning; your form should specify your clinic’s antibiotic prophylaxis protocol (if used), post-care hygiene instructions, and red flags requiring immediate contact (fever, spreading redness, purulent discharge). Hematoma (localised blood collection) may require aspiration if large or painful. Prolonged dysesthesia lasting beyond 4 weeks is uncommon but documented-your form should acknowledge it and outline when to seek specialist assessment.

State what your clinic will and won’t do. Will you offer revision treatment if results are unsatisfactory? What’s the timeline before reassessment? These boundaries, disclosed upfront, prevent misunderstandings later. Use patient portal access to allow patients to retrieve their signed consent forms and post-care instructions whenever needed.

GDPR Compliance and Digital Consent Workflows

Patient data handling during consent collection is governed by GDPR (UK Information Commissioner’s Office). A digital o-shot consent form stored in your clinic management system must meet several legal requirements.

Data minimisation: Collect only information necessary for informed consent and treatment safety. Avoid generic “marketing” permissions mixed with clinical consent. Separate the clinical consent form from any request to use patient photos before/after-these are distinct consents requiring explicit, separate agreement.

Encryption and access control: Ensure your forms platform encrypts data in transit (HTTPS) and at rest. Limit access to authorised clinical staff; reception team members typically don’t need to view signed consent documents. Audit logs should track who accessed what and when.

Retention policy: State how long you retain consent forms (typically 7 years post-treatment under UK data protection standards for aesthetic procedures, aligned with professional indemnity insurance requirements). Outline destruction methods-deletion from cloud storage, secure shredding of printed forms.

Patient rights: GDPR gives patients rights to access, correct, and delete their data. Your privacy notice should explain these rights and how patients can exercise them. For consent forms, patients can request copies; have a process to provide them within 30 days. A digital consent form solution with encryption and access controls ensures compliance automatically, so your clinical team focuses on consent quality, not compliance mechanics.

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Conclusion

An effective o-shot consent form protects both your patients and your practice. By documenting the procedure clearly, screening contraindications rigorously, disclosing risks transparently, and offering alternatives, you demonstrate clinical professionalism and medico-legal diligence. Digital workflows integrated into your medical spa management system reduce friction-patients complete forms before arrival, clinic staff review systematically, and signed documents are instantly accessible for audits or CQC inspections.

Use the template above as your starting point. Adapt it to your medical director’s protocols, your patient population’s demographics, and your clinic’s specific O-Shot technique. Update it annually as clinical evidence evolves or your patient feedback highlights gaps. A living, customised consent form is far more valuable than a generic template-it reflects your clinic’s commitment to informed, safe, ethical care.

Frequently Asked Questions