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NCT01968694 · ClinicalTrials.gov registry record · NA

Effects of Intravenous Lidocaine on Endometriosis Pain

A NA study, sponsored by Brigham and Women's Hospital.

Completed
Registry status
NA
Development phase
20
Enrollment target

NCT01968694 is a NA study that has completed, run by Brigham and Women's Hospital. The registered enrollment target is 20 participants.

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The verdict

NCT01968694, a NA study, has completed, sponsored by Brigham and Women's Hospital.

COMPLETED
Registry status
NA
Development phase
20 participants
Enrollment target

Study Summary

We are doing this research study to find out if intravenous (in your vein, "IV") lidocaine can lessen pain from endometriosis. The U.S. Food and Drug Administration (FDA) has approved intravenous lidocaine to treat irregular heart beats, but the FDA has not approved intravenous lidocaine to treat pain from endometriosis. Intravenous lidocaine has been used for more than 25 years to treat different acute and chronic pain conditions but has not yet been studied for endometriosis pain. This is a cross-over trial over two months where one month you will receive the active medication (lidocaine) and one month you will receive the active placebo (diphenhydramine, commonly known as benadryl). We will compare the effect on pain from endometriosis of lidocaine to active placebo.

Interventions

  • DRUG IV Lidocaine
  • DRUG IV diphenhydramine

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2010-12
Est. Completion 2016-06
Phase NA

Sponsor

Brigham and Women's Hospital

937 total trials

What the Registry Record Tells You About NCT01968694

The ClinicalTrials.gov registry entry for NCT01968694 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Brigham and Women's Hospital, which has 937 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which IV Lidocaine is the first listed.

NCT01968694 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01968694 about?

NCT01968694 is a clinical study titled "Effects of Intravenous Lidocaine on Endometriosis Pain". We are doing this research study to find out if intravenous (in your vein, "IV") lidocaine can lessen pain from endometriosis. The U.S. Food and Drug Administration (FDA) has approved intravenous lidocaine to treat irregular heart beats, but the FDA has not approved intravenous lidocaine to treat pa...

What is the current status of trial NCT01968694?

This trial is currently completed. It is a NA study. The enrollment target is 20 participants. The study started on 2010-12. Estimated completion is 2016-06.

What interventions are being tested in trial NCT01968694?

The interventions under investigation include: IV Lidocaine (DRUG), IV diphenhydramine (DRUG).

Who is sponsoring clinical trial NCT01968694?

This trial is sponsored by Brigham and Women's Hospital, which has 937 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.