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
| 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
| 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
| 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 yearsPopulation: 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
Email: [email protected]
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place