Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT04031716 · ClinicalTrials.gov registry record · NA
Comprehensive Study of Post-surgical Pain After Pectus or Spine Surgery
A NA study of Pain, Postoperative and Scoliosis Idiopathic, sponsored by Children's Hospital Medical Center, Cincinnati.
- Active
- Registry status
- NA
- Development phase
- 600
- Enrollment target
- 1
- Study location
NCT04031716: Active NA study of Pain, Postoperative and Scoliosis Idiopathic, sponsored by Children's Hospital Medical Center, Cincinnati.
NCT04031716 is a NA study of Pain, Postoperative and Scoliosis Idiopathic that is active but no longer recruiting, run by Children's Hospital Medical Center, Cincinnati. The registered enrollment target is 600 participants, above the 268-participant average among 113 other Pain, Postoperative trials with a reported enrollment target (124% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT04031716, a NA study of Pain, Postoperative and Scoliosis Idiopathic, is active but no longer recruiting, sponsored by Children's Hospital Medical Center, Cincinnati.
- ACTIVE NOT RECRUITING
- Registry status
- NA
- Development phase
- 600 participants
- Enrollment target
- 1
- Study location
Study Summary
This will be a prospective study to determine the association between specific genotypes, epigenetics, behavioral, social and biological factors, with the phenotypes, defined by pain perception, postoperative pain, analgesic effects, side effects to perioperative analgesics, chronic postoperative pain, and gene expression in patients following pectus excavatum repair.
Primary Outcome
Pain scores will be collected preoperatively through 1 year postoperatively
Conditions Studied
Interventions
- BEHAVIORAL Meditation
Study Locations (1)
Ohio
- Cincinnati Childrens Hospital Medical Center - Cincinnati
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 600 participants |
| Start Date | 2018-07-06 |
| Est. Completion | 2025-12-31 |
| Phase | NA |
What the registry record for NCT04031716 still lists
NCT04031716 is an interventional study that assigns participants to a tested intervention. The registered 600 participants enrollment target is mid-sized for trials with a published cap, above the 268-participant average among 113 other Pain, Postoperative trials with a reported enrollment target (124% higher).
The record links to 3 conditions, with Pain, Postoperative appearing as the primary indexed condition, and to 1 intervention - of which Meditation is the first listed.
NCT04031716 reports a single indexed study location in Ohio.
Frequently Asked Questions
What is clinical trial NCT04031716 about?
NCT04031716 is a clinical study titled "Comprehensive Study of Post-surgical Pain After Pectus or Spine Surgery". This will be a prospective study to determine the association between specific genotypes, epigenetics, behavioral, social and biological factors, with the phenotypes, defined by pain perception, postoperative pain, analgesic effects, side effects to perioperative analgesics, chronic postoperative pa...
What is the current status of trial NCT04031716?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 600 participants. The study started on 2018-07-06. Estimated completion is 2025-12-31.
What conditions does trial NCT04031716 study?
This clinical trial studies the following conditions: Pain, Postoperative, Scoliosis Idiopathic, Excavatum, Pectus.
What interventions are being tested in trial NCT04031716?
The interventions under investigation include: Meditation (BEHAVIORAL).
Who is sponsoring clinical trial NCT04031716?
This trial is sponsored by Children's Hospital Medical Center, Cincinnati, which has 571 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04031716 being conducted?
This trial has 1 study location across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Pain, Postoperative
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 NCT04031716's enrollment target sits among peer trials
600 7th of 113 higher than 107 of 113 other Pain, Postoperative trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Pain, Postoperative 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
-
Randomized Control Trial, Cryoablation as an Adjunct to Surgical Stabilization of Rib Fractures
RECRUITING · NA
-
Dance Study for Post-surgical Pain in Breast Cancer Survivors
RECRUITING · NA
-
Closed-Loop Deep Brain Stimulation for Refractory Chronic Pain
RECRUITING · NA
-
Anesthetic Optimization in Pediatric LeFort Surgeries
RECRUITING · NA
-
Latinx Children and Surgery
RECRUITING · NA
-
Trajectories of Recovery After Intravenous Propofol Versus Inhaled VolatilE Anesthesia Trial
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
- NCT00004317 · 600 participants · Phase 4
Pyrimethamine, Sulfadiazine, and Leucovorin in Treating Patients With Congenital Toxoplasmosis
- NCT00209235 · 600 participants · NA
Albright Hereditary Osteodystrophy: Natural History, Growth, and Cognitive/Behavioral Assessments
- NCT01473784 · 600 participants · NA
Transoral Robotic Surgery in Treating Patients With Benign or Malignant Tumors of the Head and Neck
- NCT01866371 · 600 participants
High Resolution Retinal Imaging
Similar registry start date
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia
- NCT07125183 · started 2026-12 · Phase 2
Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma
- NCT07292298 · started 2026-11 · Phase 2
Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates
- NCT04263285 · started 2026-10 · NA
Treatment of Depression Post-SCI