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A Study of Megestrol Acetate in HIV-Infected Children

Primary Purpose

HIV Infections

Status
Completed
Phase
Not Applicable
Locations
Puerto Rico
Study Type
Interventional
Intervention
Megestrol acetate
Sponsored by
Gamma Project - ACTU
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for HIV Infections focused on measuring Placebos, Appetite Stimulants, Megestrol Acetate, Failure to Thrive

Eligibility Criteria

6 Months - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria Patients must have: Documented HIV infection. Failure to thrive as defined by: crossing 2 percentile lines on standard weight for age curves over time or less than 5% percentile weight for age and falling from the curve or loss of 10% of baseline body weight. Resistant to oral nutritional supplementation (i.e., FTT despite a minimum 1-month trial of high-calorie oral supplements). Free of significant acute illness (mild upper respiratory tract infections allowed). Patients with chronic diarrhea allowed provided malabsorption and gastrointestinal infection ruled out. Exclusion Criteria Co-existing Condition: Patients with the following symptoms are excluded: Gastrointestinal infection or malabsorption. Significant acute illness. Any identified, untreated cause for failure to thrive other than underlying HIV infection. Medical contraindications to megestrol acetate. Patients with any of the following prior conditions or symptoms are excluded: Medical contraindications to megestrol acetate including a history of poorly-controlled hypertension, deep venous thrombosis, or heart failure. History of prior megestrol acetate therapy in the past six months.

Sites / Locations

  • Univ of Puerto Rico / Med Science Campus

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
November 2, 1999
Last Updated
June 23, 2005
Sponsor
Gamma Project - ACTU
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1. Study Identification

Unique Protocol Identification Number
NCT00002182
Brief Title
A Study of Megestrol Acetate in HIV-Infected Children
Official Title
Megestrol Acetate For Failure To Thrive In Pediatric HIV
Study Type
Interventional

2. Study Status

Record Verification Date
July 1998
Overall Recruitment Status
Completed
Study Start Date
undefined (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Gamma Project - ACTU

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to see if megestrol acetate is safe and effective in treating HIV-infected children with failure to thrive (FTT).
Detailed Description
The study design is randomized, double-blind, placebo-controlled for 12 weeks with open-label drug offered after week 12.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections
Keywords
Placebos, Appetite Stimulants, Megestrol Acetate, Failure to Thrive

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Masking
Double
Enrollment
25 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Megestrol acetate

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Months
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria Patients must have: Documented HIV infection. Failure to thrive as defined by: crossing 2 percentile lines on standard weight for age curves over time or less than 5% percentile weight for age and falling from the curve or loss of 10% of baseline body weight. Resistant to oral nutritional supplementation (i.e., FTT despite a minimum 1-month trial of high-calorie oral supplements). Free of significant acute illness (mild upper respiratory tract infections allowed). Patients with chronic diarrhea allowed provided malabsorption and gastrointestinal infection ruled out. Exclusion Criteria Co-existing Condition: Patients with the following symptoms are excluded: Gastrointestinal infection or malabsorption. Significant acute illness. Any identified, untreated cause for failure to thrive other than underlying HIV infection. Medical contraindications to megestrol acetate. Patients with any of the following prior conditions or symptoms are excluded: Medical contraindications to megestrol acetate including a history of poorly-controlled hypertension, deep venous thrombosis, or heart failure. History of prior megestrol acetate therapy in the past six months.
Facility Information:
Facility Name
Univ of Puerto Rico / Med Science Campus
City
San Juan
ZIP/Postal Code
00936
Country
Puerto Rico

12. IPD Sharing Statement

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A Study of Megestrol Acetate in HIV-Infected Children

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