CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 10 enrolled
Drug / intervention
Gabapentindrug
Likely dose
Gabapentin 100 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04345432
NCT04345432N/ACompleted

Gabapentin Treatment of Postural Tachycardia Syndrome (PoTS): a Pilot Study

Medstar Health Research Institute·interventional·Posted Apr 14, 2020·Updated Apr 14, 2020

In Brief

A clinical study evaluating Gabapentin for Postural Orthostatic Tachycardia Syndrome. Completed, enrolled 10 participants.

Detailed Summary

In this pilot study, the investigator will test the usefulness of gabapentin in treating some of the symptoms associated with POTS. Gabapentin is FDA-approved to treat epilepsy and nerve pain and works by reducing excessive activity in the nervous system. This medication has also been shown to be effective in reducing bowel discomfort in patients with irritable bowel syndrome, sleeplessness, and possibly migraine headache. The investigator has observed positive results when prescribing gabapentin off-label to alleviate photosensitivity and headaches in POTS patients. The aim of this pilot study is to better quantify what the investigator has seen and evaluate whether it merits further study in a larger group.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
Countries--
Collaborators--

Timeline

N/ACompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedApr 14, 2020
Enrollment StartJan 1, 2014
Primary CompletionSep 1, 2017
TodayJul 2, 2026
Enrollment to primary: 3.7 yearsPosted 6.2 years ago

Interventions

Gabapentindrug

Gradually increasing doses of "medication" from 100 mg on day 1 to 300 mg twice a day on day 6. On day 7, the patient received a 300-mg dose from the day 7 envelope, about two hours after a light breakfast and 1 hour before data collection. The relatively low dose and gradual titration were selected to enhance compliance and reduce adverse effects, based on a rectal mechanosensitivity study.