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NCT07064200 · ClinicalTrials.gov registry record · NA
TAP Block Timing Study
A NA study of Bariatric Surgery Patients and Bariatric or General Abdominal Surgeries, sponsored by Weill Medical College of Cornell University.
- Recruiting
- Registry status
- NA
- Development phase
- 150
- Enrollment target
- 1
- Study location
NCT07064200: Recruiting NA study of Bariatric Surgery Patients and Bariatric or General Abdominal Surgeries, sponsored by Weill Medical College of Cornell University.
NCT07064200 is a NA study of Bariatric Surgery Patients and Bariatric or General Abdominal Surgeries that is actively recruiting participants, run by Weill Medical College of Cornell University. The registered enrollment target is 150 participants, above the 93-participant average among 3 other Bariatric Surgery Patients trials with a reported enrollment target (61% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT07064200, a NA study of Bariatric Surgery Patients and Bariatric or General Abdominal Surgeries, is actively recruiting participants, sponsored by Weill Medical College of Cornell University.
- RECRUITING
- Registry status
- NA
- Development phase
- 150 participants
- Enrollment target
- 1
- Study location
Study Summary
This study investigates whether administering TAP blocks pre-incision provides superior postoperative pain control and reduces opioid use along with other medications compared to post-incision administration in patients undergoing elective abdominal surgeries.
Primary Outcome
Opioid dosage quantities will be measured in morphine milligram equivalents (MME)
Conditions Studied
Interventions
- OTHER TAP Block
Study Locations (1)
New York
- Weill Cornell Medical College - NewYork-Presbyterian Hospital - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 150 participants |
| Start Date | 2025-07-14 |
| Est. Completion | 2027-07 |
| Phase | NA |
What NCT07064200 shows while recruiting
NCT07064200 is an interventional study that assigns participants to a tested intervention. The registered 150 participants enrollment target is mid-sized for trials with a published cap, above the 93-participant average among 3 other Bariatric Surgery Patients trials with a reported enrollment target (61% higher).
The record links to 2 conditions, with Bariatric Surgery Patients appearing as the primary indexed condition, and to 1 intervention - of which TAP Block is the first listed.
NCT07064200 reports a single indexed study location in New York.
Frequently Asked Questions
What is clinical trial NCT07064200 about?
NCT07064200 is a clinical study titled "TAP Block Timing Study". This study investigates whether administering TAP blocks pre-incision provides superior postoperative pain control and reduces opioid use along with other medications compared to post-incision administration in patients undergoing elective abdominal surgeries.
What is the current status of trial NCT07064200?
This trial is currently recruiting. It is a NA study. The enrollment target is 150 participants. The study started on 2025-07-14. Estimated completion is 2027-07.
What conditions does trial NCT07064200 study?
This clinical trial studies the following conditions: Bariatric Surgery Patients, Bariatric or General Abdominal Surgeries.
What interventions are being tested in trial NCT07064200?
The interventions under investigation include: TAP Block (OTHER).
Who is sponsoring clinical trial NCT07064200?
This trial is sponsored by Weill Medical College of Cornell University, which has 701 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07064200 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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