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Antidepressant Treatment of AIDS Related Depression. - Article


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Imipramine Pamoate

Tofranil PM


Clinical Trial: Antidepressant Treatment of AIDS Related Depression.

This study has been completed.

Sponsored by: GEIGY Pharmaceuticals
Information provided by: National Institute of Mental Health (NIMH)

Purpose

To test the effectiveness treating AIDS related depression with imipramine hydrochloride.

Depression syndromes are commonly associated with chronic, disabling, and fatal diseases. Due to the relentless course of HIV infection, there is a certain reluctance to treat the associated depression. In other illness, it has been proven that treating the depression often results in improvement of overall health status.

This is a placebo controlled trial. Half of the patients are given imipramine hydrochloride every day for 6 weeks. Assessment is done by self reports and the Hamilton Depression Rating Scale. Prior to entry all patients are given a psychiatric evaluation. There is a cross over phase in which placebo non responders are entered into an open-label study and given imipramine hydrochloride.

Condition Treatment or Intervention Phase
Depression
 Drug: Imipramine hydrochloride
Phase II

MedlinePlus related topics:  Depression

Study Type: Interventional
Study Design: Treatment, Placebo Control

Further Study Details: 

To test the effectiveness treating AIDS related depression with imipramine hydrochloride.

Depression syndromes are commonly associated with chronic, disabling, and fatal diseases. Due to the relentless course of HIV infection, there is a certain reluctance to treat the associated depression. In other illness, it has been proven that treating the depression often results in improvement of overall health status.

This is a placebo controlled trial. Half of the patients are given imipramine hydrochloride every day for 6 weeks. Assessment is done by self reports and the Hamilton Depression Rating Scale. Prior to entry all patients are given a psychiatric evaluation. There is a cross over phase in which placebo non responders are entered into an open-label study and given imipramine hydrochloride.

Eligibility

Ages Eligible for Study:  18 Years   -   65 Years,  Genders Eligible for Study:  Both

Criteria

Inclusion Criteria:

  • Patient must be ambulatory and relatively good health. Even if unable to work at least able to partially care care for self and not demented.
  • May have been alcoholic or drug abuser 6 months previous.
  • Unspecified
  • CD4 Unspecified.

Exclusion Criteria:

  • Non ambulatory patients or those requiring extensive help in self care are excluded.
  • Non ambulatory patients or those requiring extensive help in self care are excluded.
  • Current alcohol or drug abuse.
  • Unspecified

Location Information


New York
      New York Hosp - Cornell Med Ctr, New York,  New York,  10021,  United States

Study chairs or principal investigators

Frances A,  Study Chair
Manning D,  Study Chair

More Information

Study ID Numbers:  87-DEP
Record last reviewed:  April 2000
Last Updated:  October 13, 2004
Record first received:  January 17, 2000
ClinicalTrials.gov Identifier:  NCT00000390
Health Authority: Unspecified
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 8, 2005


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October 11, 2008



Page Updated: June 1, 2005
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