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NCT02494336 · ClinicalTrials.gov registry record · NA
Trans-incisional vs Laparoscopic Guided Rectus Sheath Block for Pediatric Single Incision Laparoscopic Cholecystectomy
A NA study, sponsored by Johns Hopkins All Children's Hospital.
- Completed
- Registry status
- NA
- Development phase
- 48
- Enrollment target
NCT02494336 is a NA study that has completed, run by Johns Hopkins All Children's Hospital. The registered enrollment target is 48 participants.
The verdict
NCT02494336, a NA study, has completed, sponsored by Johns Hopkins All Children's Hospital.
- COMPLETED
- Registry status
- NA
- Development phase
- 48 participants
- Enrollment target
Study Summary
This is a prospective, double-blinded, randomized controlled study comparing the efficacy of trans-incisional rectus sheath block to laparoscopic guided rectus sheath block for pediatric single-incision laparoscopic cholecystectomy (SILC). umbilical hernia repair in children. Patients aged 10-21 years old undergoing SILC for cholelithiasis, cholecystitis, or biliary dyskinesia will be screened for study inclusion. Eligible patients and their parents/guardians will be approached and, if agreeable, consented for the study pre-operatively. Patients will be randomized to receive either trans-incisional rectus sheath block or intra-operative rectus sheath block under direct laparoscopic visualization. Both will be done by the attending pediatric surgeon. The patient, patient guardians, select research team members, and Post anesthesia care unit (PACU) staff will be blinded to the method of analgesic administration.
Interventions
- DRUG Ropivacaine
- PROCEDURE Trans-incisional rectus sheath block
- PROCEDURE Laparoscopic guided rectus sheath block
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 48 participants |
| Start Date | 2015-06 |
| Est. Completion | 2019-10-31 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02494336
The ClinicalTrials.gov registry entry for NCT02494336 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 48 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Johns Hopkins All Children's Hospital, which has 24 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 3 interventions - of which Ropivacaine is the first listed.
NCT02494336 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02494336 about?
NCT02494336 is a clinical study titled "Trans-incisional vs Laparoscopic Guided Rectus Sheath Block for Pediatric Single Incision Laparoscopic Cholecystectomy". This is a prospective, double-blinded, randomized controlled study comparing the efficacy of trans-incisional rectus sheath block to laparoscopic guided rectus sheath block for pediatric single-incision laparoscopic cholecystectomy (SILC). umbilical hernia repair in children. Patients aged 10-21 ye...
What is the current status of trial NCT02494336?
This trial is currently completed. It is a NA study. The enrollment target is 48 participants. The study started on 2015-06. Estimated completion is 2019-10-31.
What interventions are being tested in trial NCT02494336?
The interventions under investigation include: Ropivacaine (DRUG), Trans-incisional rectus sheath block (PROCEDURE), Laparoscopic guided rectus sheath block (PROCEDURE).
Who is sponsoring clinical trial NCT02494336?
This trial is sponsored by Johns Hopkins All Children's Hospital, which has 24 total clinical trials registered on ClinicalTrials.gov.
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