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Recruiting NCT07671430

NCT07671430 Assessment of the Benefits of Psychological Care Before Anterior Cruciate Ligament Surgery of the Knee (CLIPPER)

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Clinical Trial Summary
NCT ID NCT07671430
Status Recruiting
Phase
Sponsor GCS Ramsay Santé pour l'Enseignement et la Recherche
Condition Anxiety
Study Type INTERVENTIONAL
Enrollment 126 participants
Start Date 2026-05-07
Primary Completion 2027-06

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
A consultation with a psychologist prior to surgery

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 126 participants in total. It began in 2026-05-07 with a primary completion date of 2027-06.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The primary objective of this study is to assess the impact of a preoperative psychological consultation on postoperative pain in anxious patients undergoing primary anterior cruciate ligament reconstruction surgery.

Eligibility Criteria

Inclusion Criteria: * Patient having signed the consent form for participation in the study * Patient scheduled for first-line outpatient ACL reconstruction surgery * Patient with a score \>30 on the SFQ questionnaire (which assesses fear of surgery) * Patient with the ability to connect to the internet and follow a teleconsultation on a screen Exclusion Criteria: * Surgical history of the operated knee * History of psychiatric disorders and/or regular use of psychotropic medication * Regular use of opioid medication * Mental disability or any other reason that may hinder understanding or strict adherence to the protocol * Patient not affiliated with the French social security system * Patient under legal protection, guardianship or curatorship * Pregnant, breastfeeding or childbearing women without effective contraception * A patient who is already enrolled in another therapeutic study protocol or who has participated in another trial within the past three months

Frequently Asked Questions

Who can join the NCT07671430 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Anxiety. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07671430 currently recruiting?

Yes, NCT07671430 is actively recruiting participants. Visit ClinicalTrials.gov or contact GCS Ramsay Santé pour l'Enseignement et la Recherche to inquire about joining.

Where is the NCT07671430 trial being conducted?

This trial is being conducted at Paris, France.

Who is sponsoring the NCT07671430 clinical trial?

NCT07671430 is sponsored by GCS Ramsay Santé pour l'Enseignement et la Recherche. The trial plans to enroll 126 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology