Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT00862095 · ClinicalTrials.gov registry record · Phase 4
Medical Therapies for Chronic Post-Traumatic Headaches
A Phase 4 study, sponsored by Madigan Army Medical Center.
- Terminated
- Registry status
- Phase 4
- Development phase
- 64
- Enrollment target
NCT00862095: Clinical Trial Phase 4 study, sponsored by Madigan Army Medical Center.
NCT00862095 is a Phase 4 study that was terminated before completion, run by Madigan Army Medical Center. The registered enrollment target is 64 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (88% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00862095, a Phase 4 study, was terminated before completion, sponsored by Madigan Army Medical Center.
- TERMINATED
- Registry status
- Phase 4
- Development phase
- 64 participants
- Enrollment target
Study Summary
To determine if propranolol, amitriptyline, or topiramate decreases headache frequency in patients with chronic post-traumatic headaches.
Interventions
- DRUG Placebo
- DRUG Propranolol
- DRUG Amitriptyline
- DRUG Topiramate
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 64 participants |
| Start Date | 2008-06 |
| Est. Completion | 2013-04 |
| Phase | Phase 4 |
Why NCT00862095 stopped before completion
NCT00862095 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 64 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (88% lower).
The record links to 0 conditions, and to 4 interventions - of which Placebo is the first listed.
NCT00862095 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00862095 about?
NCT00862095 is a clinical study titled "Medical Therapies for Chronic Post-Traumatic Headaches". To determine if propranolol, amitriptyline, or topiramate decreases headache frequency in patients with chronic post-traumatic headaches.
What is the current status of trial NCT00862095?
This trial is currently terminated. It is a Phase 4 study. The enrollment target is 64 participants. The study started on 2008-06. Estimated completion is 2013-04.
What interventions are being tested in trial NCT00862095?
The interventions under investigation include: Placebo (DRUG), Propranolol (DRUG), Amitriptyline (DRUG), Topiramate (DRUG).
Who is sponsoring clinical trial NCT00862095?
This trial is sponsored by Madigan Army Medical Center, which has 22 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00862095's enrollment target sits among peer trials
64 1098th of 2000 higher than 895 of 2,000 other Phase 4 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 4 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
- NCT01853631 · 64 participants · Phase 1
Activated T-Cells Expressing 2nd or 3rd Generation CD19-Specific CAR, Advanced B-Cell NHL, ALL, and CLL (SAGAN)
- NCT03739502 · 64 participants · Phase 2
A Randomized Phase II Study of Hyperbaric Oxygen in Improving Engraftment in Umbilical Cord Blood Stem Cell Transplant
- NCT03739814 · 64 participants · Phase 2
Inotuzumab Ozogamicin and Blinatumomab With or Without Ponatinib in Treating Patients With Newly Diagnosed, Recurrent, or Refractory CD22-Positive B-Lineage Acute Lymphoblastic Leukemia
- NCT03866408 · 64 participants · Early Phase 1
Insulin Regulation of Lipolysis and Lipolysis Proteins
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