Excessive Sweating Caused by Antidepressants: Measurement and Treatment With Terazosin (ADIES)

This study has been completed.
Sponsor:
Collaborator:
National Alliance for Research on Schizophrenia and Depression
Information provided by:
Thomas Jefferson University
ClinicalTrials.gov Identifier:
NCT00449683
First received: March 19, 2007
Last updated: February 7, 2011
Last verified: February 2011

March 19, 2007
February 7, 2011
March 2007
Not Provided
  • To study whether terazosin 1 to 4 mg/ day is effective in reducing antidepressant-induced sweating
  • To test a novel device for ambulatory monitoring of sweating which is required to study this phenomenon since ADIES is usually episodic
Same as current
Complete list of historical versions of study NCT00449683 on ClinicalTrials.gov Archive Site
  • To determine if the severity of sweating at baseline is correlated with baseline urinary norepinephrine levels
  • To determine if response to treatment correlated with baseline urinary norepinephrine levels and with changes in these levels during the study.
Same as current
Not Provided
Not Provided
 
Excessive Sweating Caused by Antidepressants: Measurement and Treatment With Terazosin
Antidepressant Induced Excessive Sweating: Measurement and Treatment With Terazosin

The study consists of measurement of antidepressant-induced excessive sweating and its treatment with an experimental medication, terazosin (approved for hypertension), that will be added to the antidepressant. This study is for people who take an antidressant due to a depressive disorder. This is an open-label study (no placebo group) that will last 5 weeks, with one week of baseline measurement and four weeks of treatment with the study medication. The study is based on the hypothesis that terazosin will be effective in reducing the severity of excessive sweating caused by antidepressant treatment, and will have minimal side-effects.

Not Provided
Interventional
Phase 4
Allocation: Non-Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Hyperhidrosis
Drug: terazosin
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
20
Not Provided
Not Provided

Inclusion Criteria:

  1. Age 18 - 75 years
  2. Clinical diagnosis of a Depressive disorder (Diagnostic and Statistical Manual of Mental Disorders - IV-TR)
  3. Presence of excessive sweating by self-report
  4. The excessive sweating started after initiation of an antidepressant and, if treatment with the antidepressant was interrupted, did not persist for more than 4 weeks during that interruption
  5. Treatment with the antidepressant is deemed to be clinically necessary due to substantial benefit from this antidepressant, and failure to respond to or tolerate an alternative
  6. Excessive sweating has persisted for at least 4 weeks prior to baseline assessment
  7. The excessive sweating is rated by the patient as at least moderately bothersome.
  8. Episodes of excessive sweating occur at least twice a week for last 4 weeks

Exclusion Criteria:

  1. Presence of another known disease that could potentially cause excessive sweating
  2. Failure to respond to antiadrenergic (reducing activity of the sympathetic nervous system) treatment in the past
  3. Blood pressure less than 110 mm Hg systolic at the screening or baseline visits
  4. Orthostatic hypotension by history or on assessment at the screening or baseline visits (defined as a decrease of 10 mm Hg or greater after standing for 2 minutes).
  5. Current antihypertensive treatment
  6. History of significant cardiac disease, including coronary artery disease
  7. Current use of phosphodiesterase type 5 inhibitors: sildenafil (ViagraTM), tadalafil (CialisTM), or vardenafil (LevitraTM)
  8. History of priapism (persistent and painful erection)
Both
18 Years to 75 Years
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00449683
06F.275
No
Not Provided
Thomas Jefferson University
National Alliance for Research on Schizophrenia and Depression
Principal Investigator: Rajnish Mago, MD Thomas Jefferson University
Thomas Jefferson University
February 2011

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP