Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02947633 · ClinicalTrials.gov registry record · NA

Sciatic Technique Comparison of Nerve Blockade for Pain Control Following Hamstring Autograft Harvest in Adolescents

A NA study, sponsored by Children's Hospital Medical Center, Cincinnati.

Completed
Registry status
NA
Development phase
141
Enrollment target

NCT02947633: Completed NA study, sponsored by Children's Hospital Medical Center, Cincinnati.

NCT02947633 is a NA study that has completed, run by Children's Hospital Medical Center, Cincinnati. The registered enrollment target is 141 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (90% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02947633, a NA study, has completed, sponsored by Children's Hospital Medical Center, Cincinnati.

COMPLETED
Registry status
NA
Development phase
141 participants
Enrollment target

Study Summary

The purpose of this research is to compare the effect of single-injection sciatic PNB to continuous sciatic PNB on 1) postoperative pain control as measured by self-reported pain scores, pain medication use, and unplanned hospital admission due to poor pain control, 2) active knee flexion, and 3) patient satisfaction with pain control following ACL reconstruction with a hamstring autograft. The results of this research have the potential to positively impact pain control for the adolescent population undergoing this surgical procedure and foster responsible utilization of limited resources.

Primary Outcome

Guardian collects Numeric Rating Scale (NRS) pain score. The range is 0 - 10. 0 being no pain, 10 being the worst pain imaginable.

Interventions

  • DRUG Single-injection sciatic PNB
  • DRUG Continuous sciatic PNB

Trial Details

FieldValue
Enrollment Target 141 participants
Start Date 2015-03
Est. Completion 2024-04
Phase NA

What the finished NCT02947633 record still lists

NCT02947633 is an interventional study that assigns participants to a tested intervention. The registered 141 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 (90% lower).

The record links to 0 conditions, and to 2 interventions - of which Single-injection sciatic PNB is the first listed.

NCT02947633 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02947633 about?

NCT02947633 is a clinical study titled "Sciatic Technique Comparison of Nerve Blockade for Pain Control Following Hamstring Autograft Harvest in Adolescents". The purpose of this research is to compare the effect of single-injection sciatic PNB to continuous sciatic PNB on 1) postoperative pain control as measured by self-reported pain scores, pain medication use, and unplanned hospital admission due to poor pain control, 2) active knee flexion, and 3) pa...

What is the current status of trial NCT02947633?

This trial is currently completed. It is a NA study. The enrollment target is 141 participants. The study started on 2015-03. Estimated completion is 2024-04.

What interventions are being tested in trial NCT02947633?

The interventions under investigation include: Single-injection sciatic PNB (DRUG), Continuous sciatic PNB (DRUG).

Who is sponsoring clinical trial NCT02947633?

This trial is sponsored by Children's Hospital Medical Center, Cincinnati, which has 571 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02947633's enrollment target sits among peer trials

141 712th of 2000 higher than 1,288 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT03042962 · 141 participants

    Brain Networks in Dystonia

  • NCT04378439 · 141 participants · NA

    Appalachian Partnership to Reduce Disparities (Aim 2)

  • NCT04775485 · 141 participants · Phase 2

    A Study to Evaluate Tovorafenib in Pediatric and Young Adult Participants With Relapsed or Progressive Low-Grade Glioma and Advance Solid Tumors

  • NCT05040360 · 141 participants · Phase 2

    Testing the Use of Chemotherapy After Surgery for High-Risk Pancreatic Neuroendocrine Tumors

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT02947633, the US trial registry maintained by the National Library of Medicine. NCT02947633 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.