CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 96 enrolled
Drug / intervention
TRH (Thyrotropin Releasing Hormone)drug
Likely dose
Not stated in record
Key inclusion· 1
  • Adults and children requiring dynamic testing of the hypothalamic-pituitary axis for evaluation of pituitary reserve, inconsistent thyroid function tests, inappropriate TSH secretion, or pre- and post-operative evaluation of pituitary adenomas
Key exclusion· 7
  • Uncontrolled hypertension
  • Uncontrolled seizure disorder
  • Unstable coronary disease
  • Known allergy to TRH

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00054756
NCT00054756Phase 2Completed

Study of Thyrotropin Releasing Hormone in Patients With Thyroid or Pituitary Abnormalities

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)·interventional·Posted Feb 10, 2003·Updated Aug 8, 2018

In Brief

A Phase 2 clinical trial evaluating TRH (Thyrotropin Releasing Hormone) for Healthy and 2 related conditions. Completed, enrolled 96 participants across 1 site.

Detailed Summary

This study will determine the safety and activity of a new formulation of thyrotropin-releasing hormone (TRH), a drug used for diagnosing and evaluating patients with certain thyroid gland abnormalities. Normal thyroid gland function depends on proper chemical signaling between the thyroid gland, the hypothalamus (the part of the brain where TRH is made), and the pituitary (another part of the brain). The TRH test helps assess this interaction. Production of the only FDA-approved preparation of TRH was stopped in July 2002. As a result, to have a continuous source of TRH available for NIH clinical and research purposes, the NIH Clinical Center (CC) Pharmacy Department produced a pharmaceutical grade formulation of TRH for patient use. This study will test the CC formulation in healthy volunteers to show that its activity and side effects are similar to those of the previously available commercial test preparation. It will then be studied in CC patients for whom the diagnostic test is recommended. Healthy volunteers between 18 and 65 years of age and all patients requiring TRH evaluation of hypothalamic-pituitary-thyroid gland interaction may be eligible for this study. Patients include those with pituitary reserve, inconsistent thyroid function test, inappropriate TSH secretion, or pre- and post-operative evaluation of pituitary tumors. Normal volunteers will be screened with a medical history, physical examination, and blood tests. Women of child-bearing potential will be given a pregnancy test; pregnant and breast-feeding women may not participate. The TRH test procedure will be the same for healthy volunteers and patients. All participants fast from midnight before the morning of the test. In the morning, a catheter (flexible plastic tube) is inserted into an arm vein for easy injection of the TRH and collection of blood samples. Blood pressure is monitored before and during the test. A blood sample is drawn, and then TRH is given through the catheter over a 1-minute period. Another nine blood samples are collected over a 3-hour period from the time of the TRH injection for measuring levels of various hormones. A total of less than 4 tablespoons of blood is taken for the test.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
2003200420052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedFeb 10, 2003
Enrollment StartFeb 7, 2003
Primary CompletionSep 26, 2014
TodayJul 2, 2026
Enrollment to primary: 11.6 yearsPosted 23.4 years ago

Interventions

TRH (Thyrotropin Releasing Hormone)drug