Trial Outcomes & Findings for Six Month Treatment of Growth Hormone Releasing Hormone (GHRH) in the Elderly (NCT NCT00807365)

NCT ID: NCT00807365

Last Updated: 2017-04-27

Results Overview

Recruitment status

TERMINATED

Study phase

PHASE2

Target enrollment

5 participants

Primary outcome timeframe

2 years

Results posted on

2017-04-27

Participant Flow

Participant milestones

Participant milestones
Measure
GHRH
Growth Hormone-Releasing Hormone GHRH: GHRH administered subcutaneously at 2.0 mg/kg/dose bolus each night at 11:00 Post Meridian (PM), 1:00 Ante Meridian (AM), 3:00 AM, \& 5:00 AM for 6 months.
Overall Study
STARTED
5
Overall Study
COMPLETED
0
Overall Study
NOT COMPLETED
5

Reasons for withdrawal

Reasons for withdrawal
Measure
GHRH
Growth Hormone-Releasing Hormone GHRH: GHRH administered subcutaneously at 2.0 mg/kg/dose bolus each night at 11:00 Post Meridian (PM), 1:00 Ante Meridian (AM), 3:00 AM, \& 5:00 AM for 6 months.
Overall Study
Study Terminated
5

Baseline Characteristics

Six Month Treatment of Growth Hormone Releasing Hormone (GHRH) in the Elderly

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
GHRH
n=5 Participants
Growth Hormone-Releasing Hormone GHRH: GHRH administered subcutaneously at 2.0 mg/kg/dose bolus each night at 11:00 PM, 1:00 AM, 3:00 AM, \& 5:00 AM for 6 months.
Age, Categorical
<=18 years
0 Participants
n=5 Participants
Age, Categorical
Between 18 and 65 years
0 Participants
n=5 Participants
Age, Categorical
>=65 years
5 Participants
n=5 Participants
Sex: Female, Male
Female
2 Participants
n=5 Participants
Sex: Female, Male
Male
3 Participants
n=5 Participants
Region of Enrollment
United States
5 participants
n=5 Participants

PRIMARY outcome

Timeframe: 2 years

Population: Study terminated prior to collection of data

Outcome measures

Outcome data not reported

Adverse Events

GHRH

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Johns Hopkins ClinicalTrials.gov Program

Johns Hopkins University

Phone: 4105506484

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place