Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT01693588 · ClinicalTrials.gov registry record · NA
Study of a Multimodality Pain Management Protocol on Postoperative Neurosurgical Pain
A NA study of Pain and Postoperative Pain, sponsored by University of Florida.
- Completed
- Registry status
- NA
- Development phase
- 94
- Enrollment target
- 1
- Study location
NCT01693588: Completed NA study of Pain and Postoperative Pain, sponsored by University of Florida.
NCT01693588 is a NA study of Pain and Postoperative Pain that has completed, run by University of Florida. The registered enrollment target is 94 participants, below the 304-participant average among 374 other Pain trials with a reported enrollment target (69% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01693588, a NA study of Pain and Postoperative Pain, has completed, sponsored by University of Florida.
- COMPLETED
- Registry status
- NA
- Development phase
- 94 participants
- Enrollment target
- 1
- Study location
Study Summary
High levels of postoperative pain are associated with an increased risk of lung and heart complications, are the most common reason for delayed discharge or for unexpected hospital admission after ambulatory surgery, and are responsible for prolonged recovery after inpatient surgery. Furthermore both neuropathic pain and post surgical pain inhibit weight gain and may have an impact on the patient's nutrition post operatively. The purpose of this study is to evaluate the effectiveness of a multimodality pain management protocol on postoperative neurosurgical pain.
Primary Outcome
The Visual Analogue Scale measures the severity of pain on a continuous scale from 0 (no pain) to 10 (worst possible pain).
Conditions Studied
Interventions
- OTHER Pain Management Bundle
Study Locations (1)
Florida
- University of Florida - Gainesville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 94 participants |
| Start Date | 2012-10 |
| Est. Completion | 2013-08 |
| Phase | NA |
What the finished NCT01693588 record still lists
NCT01693588 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 94 participants, a relatively small participant target, below the 304-participant average among 374 other Pain trials with a reported enrollment target (69% lower).
The record links to 4 conditions, with Pain appearing as the primary indexed condition, and to 1 intervention - of which Pain Management Bundle is the first listed.
NCT01693588 reports a single indexed study location in Florida.
Frequently Asked Questions
What is clinical trial NCT01693588 about?
NCT01693588 is a clinical study titled "Study of a Multimodality Pain Management Protocol on Postoperative Neurosurgical Pain". High levels of postoperative pain are associated with an increased risk of lung and heart complications, are the most common reason for delayed discharge or for unexpected hospital admission after ambulatory surgery, and are responsible for prolonged recovery after inpatient surgery. Furthermore bot...
What is the current status of trial NCT01693588?
This trial is currently completed. It is a NA study. The enrollment target is 94 participants. The study started on 2012-10. Estimated completion is 2013-08.
What conditions does trial NCT01693588 study?
This clinical trial studies the following conditions: Pain, Postoperative Pain, Surgical Pain, Neurosurgical Pain.
What interventions are being tested in trial NCT01693588?
The interventions under investigation include: Pain Management Bundle (OTHER).
Who is sponsoring clinical trial NCT01693588?
This trial is sponsored by University of Florida, which has 1,106 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01693588 being conducted?
This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Pain
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 NCT01693588's enrollment target sits among peer trials
94 178th of 374 higher than 197 of 374 other Pain trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Pain 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
-
Postoperative Pain After Activation of Irrigant
RECRUITING · NA
-
Neural Mechanisms of Immersive Virtual Reality in Chronic Pain (VR TMD EEG)
RECRUITING · NA
-
Pain With Dementia
RECRUITING · NA
-
Oklahoma Study of Native American Pain Risk IV: Smoking Cessation and Pain
RECRUITING · NA
-
Peer Support for Adolescents and Emerging Adults With Sickle Cell Pain
RECRUITING · NA
-
TENS Analgesia During Outpatient Urethral Bulking for Stress Urinary Incontinence.
RECRUITING · NA
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
- NCT03747146 · 94 participants · NA
Enhanced Recovery After Surgery (ERAS) Total Knee Replacement (TKR) With a Transitional Pain Service
- NCT04061421 · 94 participants · Phase 1
Active Myeloid Target Compound Combinations in MDS/MPN Overlap Syndromes Overlap Syndromes (ABNL-MARRO)
- NCT04205968 · 94 participants · Phase 2
Ramucirumab and Paclitaxel or FOLFIRI in Advanced Small Bowel Cancers
- NCT04464759 · 94 participants · Phase 1
A Study of Nivolumab and Hydroxychloroquine or Nivolumab/Ipilimumab and Hydroxychloroquine in Advanced Melanoma
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