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NCT07461558 · ClinicalTrials.gov registry record · NA
Watchful Waiting Versus Immediate Repair for Occult Contralateral Inguinal Hernias.
A NA study of Inguinal Hernia Bilateral and Inguinal Hernia Unilateral, sponsored by Northwestern University.
- Recruiting
- Registry status
- NA
- Development phase
- 380
- Enrollment target
- 1
- Study location
NCT07461558: Recruiting NA study of Inguinal Hernia Bilateral and Inguinal Hernia Unilateral, sponsored by Northwestern University.
NCT07461558 is a NA study of Inguinal Hernia Bilateral and Inguinal Hernia Unilateral that is actively recruiting participants, run by Northwestern University. The registered enrollment target is 380 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (73% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT07461558, a NA study of Inguinal Hernia Bilateral and Inguinal Hernia Unilateral, is actively recruiting participants, sponsored by Northwestern University.
- RECRUITING
- Registry status
- NA
- Development phase
- 380 participants
- Enrollment target
- 1
- Study location
Study Summary
This study will compare two ways of managing a small, hidden hernia that can sometimes be found during minimally invasive surgery to repair a hernia on one side of the groin. Occasionally while fixing the known hernia, the surgeon discovers a small hernia on the other side that has not caused any symptoms. Surgeons do not agree on the best way to handle these hernias. Some believe it should be repaired right away during the same operation to prevent it from getting bigger or from causing symptoms later, which could require another surgery. Others believe it is better to leave it alone since it is not causing problems and groin hernia surgery carries risks including long-term pain. This study will randomly assign patients, if a hidden hernia is found during surgery, to either having it repaired immediately or to have it monitored over time. Patients will be followed up at 30 days, 1 year and 2 years following surgery. The researchers will compare recovery and quality of life between the two groups. For those in the monitoring group, the study will also track whether the hidden hernia causes symptoms or eventually needs surgery. The goal is to determine whether repairing the hidden hernia right away is as safe and effective as watching and waiting, so doctors and patients can make more informed decisions in the future.
Primary Outcome
At 30 days postoperatively, patients will see their operating surgeon and will undergo a physical exam and complete a EuraHS survey as is standard of care. The EuraHS Quality of Life Score, validated for inguinal hernia patients, allows quantification of pain, physical restriction, and cosmetic satisfaction-domains directly affected by surgical intervention.
Conditions Studied
Interventions
- PROCEDURE surgery (any volume) and / or pharmaceuticals treatment initiated or planned or only dynamic observation, in accordance with current clinical guidelines
- PROCEDURE Watchful waiting with supportive care
Study Locations (1)
Illinois
- Northwestern Memorial Hospital - Chicago
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 380 participants |
| Start Date | 2026-04 |
| Est. Completion | 2029-04 |
| Phase | NA |
What NCT07461558 shows while recruiting
NCT07461558 is an interventional study that assigns participants to a tested intervention. The registered 380 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (73% lower).
The record links to 2 conditions, with Inguinal Hernia Bilateral appearing as the primary indexed condition, and to 2 interventions - of which surgery (any volume) and / or pharmaceuticals treatment initiated or planned or only dynamic observation, in accordance with current clinical guidelines is the first listed.
NCT07461558 reports a single indexed study location in Illinois.
Frequently Asked Questions
What is clinical trial NCT07461558 about?
NCT07461558 is a clinical study titled "Watchful Waiting Versus Immediate Repair for Occult Contralateral Inguinal Hernias.". This study will compare two ways of managing a small, hidden hernia that can sometimes be found during minimally invasive surgery to repair a hernia on one side of the groin. Occasionally while fixing the known hernia, the surgeon discovers a small hernia on the other side that has not caused any sy...
What is the current status of trial NCT07461558?
This trial is currently recruiting. It is a NA study. The enrollment target is 380 participants. The study started on 2026-04. Estimated completion is 2029-04.
What conditions does trial NCT07461558 study?
This clinical trial studies the following conditions: Inguinal Hernia Bilateral, Inguinal Hernia Unilateral.
What interventions are being tested in trial NCT07461558?
The interventions under investigation include: surgery (any volume) and / or pharmaceuticals treatment initiated or planned or only dynamic observation, in accordance with current clinical guidelines (PROCEDURE), Watchful waiting with supportive care (PROCEDURE).
Who is sponsoring clinical trial NCT07461558?
This trial is sponsored by Northwestern University, which has 1,209 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07461558 being conducted?
This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT07461558's enrollment target sits among peer trials
380 273rd of 2000 higher than 1,727 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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