Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT01110759 · ClinicalTrials.gov registry record
Medical Review: Hand Surgery After Local Block Versus Non-block
A clinical trial, sponsored by Cedars-Sinai Medical Center.
- Completed
- Registry status
- 200
- Enrollment target
NCT01110759: Completed study, sponsored by Cedars-Sinai Medical Center.
NCT01110759 is a clinical trial that has completed, run by Cedars-Sinai Medical Center. The registered enrollment target is 200 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01110759 has completed, sponsored by Cedars-Sinai Medical Center.
- COMPLETED
- Registry status
- 200 participants
- Enrollment target
Study Summary
In this study, the effects of local block vs non block will be assessed with respect to postoperative outcomes (such as pain score, and recovery profiles) in outpatients after hand surgery.
Primary Outcome
1. Severity of the pain experienced before patient left the surgery center and after patient arrived at home 2. Pain medication (amounts of opioids and non opioids pills) required d)Time to suffer pain at the surgical site (hand) (days, weeks, or months)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 200 participants |
| Start Date | 2009-08 |
| Est. Completion | 2011-07 |
What the finished NCT01110759 record still lists
NCT01110759 is an observational study that tracks outcomes without assigning an intervention. The registered 200 participants enrollment target is mid-sized for trials with a published cap.
The record links to 0 conditions, and to 0 interventions.
NCT01110759 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01110759 about?
NCT01110759 is a clinical study titled "Medical Review: Hand Surgery After Local Block Versus Non-block". In this study, the effects of local block vs non block will be assessed with respect to postoperative outcomes (such as pain score, and recovery profiles) in outpatients after hand surgery.
What is the current status of trial NCT01110759?
This trial is currently completed. The enrollment target is 200 participants. The study started on 2009-08. Estimated completion is 2011-07.
Who is sponsoring clinical trial NCT01110759?
This trial is sponsored by Cedars-Sinai Medical Center, which has 339 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
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
- NCT00107289 · 200 participants · Phase 2
Iodine I 131 Metaiodobenzylguanidine in Treating Patients With Recurrent, Progressive, or Refractory Neuroblastoma or Malignant Pheochromocytoma or Paraganglioma
- NCT00109174 · 200 participants · NA
MRS Measurement of Glutamate and GABA Metabolism in Brain
- NCT00177268 · 200 participants
Blood, Urine, and Tissue Collection for Cutaneous Lymphoma, Eczema, and Atopic Dermatitis Research
- NCT00493688 · 200 participants
A Study to Determine Whether Perioperative Energy Dynamics Correlates With Postoperative Outcomes
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