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Growth Hormone Releasing Hormone Analog

Immediate group for Mild Cognitive Impairment

Phase 2
Waitlist Available
Led By Fred Sattler, MD
Research Sponsored by University of California, San Diego
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 months and 12 months
Awards & highlights

Study Summary

This trial will test if a combination of tesamorelin and a text-messaging application can improve memory and thinking in HIV patients.

Eligible Conditions
  • Mild Cognitive Impairment

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 months and 12 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 6 months and 12 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Neurocognitive performance
Secondary outcome measures
Biomarkers of visceral adipose tissue (VAT)-related inflammation and immune activation, metabolic parameters, and neuronal integrity

Trial Design

2Treatment groups
Active Control
Placebo Group
Group I: Immediate groupActive Control1 Intervention
1.4mg of tesamorelin is injected once a day for 6 months, then no treatment is given for 6 months
Group II: Deferred groupPlacebo Group1 Intervention
No treatment is given for 6 months, then 1.4mg of tesamorelin is injected once a day for 6 months

Find a Location

Who is running the clinical trial?

University of California, San DiegoLead Sponsor
1,124 Previous Clinical Trials
1,552,818 Total Patients Enrolled
University of Southern CaliforniaOTHER
906 Previous Clinical Trials
1,596,084 Total Patients Enrolled
University of California, San FranciscoOTHER
2,507 Previous Clinical Trials
15,238,467 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

How many study participants have enrolled in the trial thus far?

"Affirmative. Clinicaltrials.gov reveals that this trial, first promulgated on February 15th 2017 and most recently modified on July 6th 2022, is actively recruiting 100 participants across 4 sites."

Answered by AI

Is the Immediate group a reliable option for those seeking treatment?

"Immediate group's safety has been assessed with a rating of 2, indicating there is some data available on this intervention's security but no evidence testifying to its efficacy."

Answered by AI

What other investigations have been conducted to explore the effects of Immediate group?

"At present, Immediate group is being researched in 4 active clinical trials. None of the studies are currently in Phase 3. Most of these studies take place within New york City limits, however there are also 8 other sites around the country which have dedicated research projects concerning this medication."

Answered by AI

Does the research team currently need additional participants for their project?

"As publicly documented on clinicaltrials.gov, this trial is currently open to enrollment and has been since February 15th 2017. The information was most recently updated on July 6th 2022."

Answered by AI

How many healthcare facilities are trialing this experiment?

"This medical trial is being conducted in four distinct locations, including the HIV Neurobehavioral Research Program (HNRP) based in San Diego, Keck School of Medicine of the University of Southern California located in Los Angeles and University of California, San Francisco situated in San Francisco. Additionally there are other research sites participating."

Answered by AI
~9 spots leftby May 2025