NCT07608653 Outcomes of Laparoscopic Keyhole Surgery (TAPP) for Recurrent Inguinal Hernia
| NCT ID | NCT07608653 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Sohag University |
| Condition | Recurrant Inguinal Hernia |
| Study Type | INTERVENTIONAL |
| Enrollment | 10 participants |
| Start Date | 2026-04-01 |
| Primary Completion | 2026-07-01 |
Eligibility & Interventions
Eligibility Fast-Check
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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 10 participants in total. It began in 2026-04-01 with a primary completion date of 2026-07-01.
⚠ 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 goal of this clinical trial is to learn if a laparoscopic surgery called Transabdominal Preperitoneal (TAPP) repair is safe and works well for adults with a recurrent inguinal hernia (a groin hernia that has returned after a previous operation). The main questions it aims to answer are: Does the TAPP technique lower the number of complications after surgery? How well do participants recover during the early postoperative period and long-term follow-up? Fixing a hernia that has returned is hard because of old scar tissue. In this study, researchers will use the TAPP technique to work through a different layer of tissue to provide a stronger repair. Participants will: Undergo the TAPP laparoscopic surgery for their recurrent hernia. Visit the clinic for close health monitoring shortly after surgery. Complete regular follow-up checkups to track their long-term recovery.
Eligibility Criteria
Inclusion Criteria: * Adult patients. Patients diagnosed with recurrent inguinal hernia. Patients fit for general anesthesia. Patients who provide informed consent. Exclusion Criteria: * Non recurrent inguinal hernia Patients with complicated inguinal hernia. Patients unfit for general anesthesia. Patients refusing participation in the study.
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07608653 clinical trial?
This trial is open to participants of all sexes, studying Recurrant Inguinal Hernia. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07608653 currently recruiting?
Yes, NCT07608653 is actively recruiting participants. Contact the research team at marwaelkholy93@gmail.com for enrollment information.
Where is the NCT07608653 trial being conducted?
This trial is being conducted at Sohag, Egypt.
Who is sponsoring the NCT07608653 clinical trial?
NCT07608653 is sponsored by Sohag University. The trial plans to enroll 10 participants.