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NCT00905320 · ClinicalTrials.gov registry record · NA
Hernia Repair With or Without Sutures
A NA study of Hernia, sponsored by Indiana University.
- Completed
- Registry status
- NA
- Development phase
- 58
- Enrollment target
- 1
- Study location
NCT00905320: Completed NA study of Hernia, sponsored by Indiana University.
NCT00905320 is a NA study of Hernia that has completed, run by Indiana University. The registered enrollment target is 58 participants, below the 197-participant average among 11 other Hernia trials with a reported enrollment target (71% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00905320, a NA study of Hernia, has completed, sponsored by Indiana University.
- COMPLETED
- Registry status
- NA
- Development phase
- 58 participants
- Enrollment target
- 1
- Study location
Study Summary
This is a randomized study between two accepted techniques of mesh fixation for laparoscopic hernia repair.
Primary Outcome
Short-Form McGill Pain Questionnaire (SFMP)
Conditions Studied
Interventions
- PROCEDURE Metallic Fasteners and Sutures
- PROCEDURE Metallic Fasteners Alone
Study Locations (1)
Indiana
- Indiana University - Indianapolis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 58 participants |
| Start Date | 2009-09 |
| Est. Completion | 2018-11-21 |
| Phase | NA |
What the finished NCT00905320 record still lists
NCT00905320 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 58 participants, a relatively small participant target, below the 197-participant average among 11 other Hernia trials with a reported enrollment target (71% lower).
The record links to 1 condition, with Hernia appearing as the primary indexed condition, and to 2 interventions - of which Metallic Fasteners and Sutures is the first listed.
NCT00905320 reports a single indexed study location in Indiana.
Frequently Asked Questions
What is clinical trial NCT00905320 about?
NCT00905320 is a clinical study titled "Hernia Repair With or Without Sutures". This is a randomized study between two accepted techniques of mesh fixation for laparoscopic hernia repair.
What is the current status of trial NCT00905320?
This trial is currently completed. It is a NA study. The enrollment target is 58 participants. The study started on 2009-09. Estimated completion is 2018-11-21.
What conditions does trial NCT00905320 study?
This clinical trial studies the following conditions: Hernia.
What interventions are being tested in trial NCT00905320?
The interventions under investigation include: Metallic Fasteners and Sutures (PROCEDURE), Metallic Fasteners Alone (PROCEDURE).
Who is sponsoring clinical trial NCT00905320?
This trial is sponsored by Indiana University, which has 890 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00905320 being conducted?
This trial has 1 study location across Indiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Hernia
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT00905320's enrollment target sits among peer trials
58 9th of 11 higher than 3 of 11 other Hernia trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Hernia 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
-
Prospective Registry for Long-term Outcomes Following FETO in Severe Left and Right CDH
RECRUITING · NA
-
Transorb™ Self-Gripping Resorbable Mesh in High-risk Subjects Undergoing Open Repair of Ventral Hernia
ACTIVE NOT RECRUITING · NA
-
Pilot Trial of Abdominal Core Rehabilitation To Improve Outcomes After Ventral Hernia Repair
ACTIVE NOT RECRUITING · NA
-
Evaluate and Compare the Rate of Para-Stomal Herniation After Permanent Stoma Formation
COMPLETED · NA
-
Evaluation of Surgisis Gold Graft for Incision Reinforcement After Open Bariatric Surgery
COMPLETED · NA
-
CT and Radiologist RCT
COMPLETED · NA
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