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New treatment option for Inguinal Hernia
Official title The Importance of Preserving the Round Ligament in the Repair of Inguinal Hernias in Women
ClinicalTrials.gov ID: NCT06786702
What this study is testing
- What it's testing
- The aim of this study is to evaluate the impact of preserving or not preserving the round ligament during laparoscopic Trans Abdominal Pre-Peritoneal (TAPP) hernia repair on postoperative outcomes in female patients. Specifically, the study will compare outcomes such as postoperative pain, seroma, hematoma, prolapsus of uterina , recurrence rates, and quality of life between patients whose round ligament was preserved versus those whose ligament was cut.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 70, women only
You may be able to join if
- For patients applying to the General Surgery Clinic of Basaksehir Cam Sakura City Hospital:
- Age Range: Female patients aged between 18 and 70 years.
- Type of Hernia: Patients with inguinal, direct or indirect, femoral, and obturator hernias.
- Surgical Indication: Patients indicated for TAPP (Transabdominal Preperitoneal) surgery.
- Consent: Patients who consent to participate in the study.
You likely can't join if
- Age: Female patients under 18 years old or over 70 years old.
- Surgical Technique: Patients who are operated on with techniques other than TAPP (e.g., TEP, conventional surgery).
- Hernia Type: Patients with strangulated or incarcerated hernias.
- Hernia Location: Patients with hernias outside the groin region.
- Surgical Site: Surgeries performed in different clinics.
- Gender: Male patients.
See the full eligibility criteria
- For patients applying to the General Surgery Clinic of Basaksehir Cam Sakura City Hospital:
- Age Range: Female patients aged between 18 and 70 years.
- Type of Hernia: Patients with inguinal, direct or indirect, femoral, and obturator hernias.
- Surgical Indication: Patients indicated for TAPP (Transabdominal Preperitoneal) surgery.
- Consent: Patients who consent to participate in the study.
- General Anesthesia: Patients who are suitable for general anesthesia.
- Follow-up: Patients who attend follow-up appointments regularly.
- Age: Female patients under 18 years old or over 70 years old.
- Surgical Technique: Patients who are operated on with techniques other than TAPP (e.g., TEP, conventional surgery).
- Hernia Type: Patients with strangulated or incarcerated hernias.
- Hernia Location: Patients with hernias outside the groin region.
- Surgical Site: Surgeries performed in different clinics.
- Gender: Male patients.
The study team makes the final eligibility decision.
Where it's taking place
- Istanbul, Başakşehir, Turkey (Türkiye)
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling female, 18 years to 70 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Istanbul, Başakşehir, Turkey (Türkiye). Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.