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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00000323
Other study ID # NIDA-10753-1
Secondary ID R01-10753-1
Status Completed
Phase Phase 1
First received September 20, 1999
Last updated January 11, 2017
Start date July 1996
Est. completion date December 1998

Study information

Verified date May 2004
Source National Institute on Drug Abuse (NIDA)
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Observational

Clinical Trial Summary

The purpose of this study is to characterize the effects of enadoline compared to hydromorphone and butorphanol.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date December 1998
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 21 Years to 50 Years
Eligibility Inclusion Criteria:

opiate experienced, healthy

Exclusion Criteria:

physical dependence on opioids, barbiturates or alcohol

Study Design

N/A


Related Conditions & MeSH terms


Locations

Country Name City State
United States Johns Hopkins University (BPRU) Bayview Campus Baltimore Maryland

Sponsors (1)

Lead Sponsor Collaborator
National Institute on Drug Abuse (NIDA)

Country where clinical trial is conducted

United States, 

References & Publications (1)

Walsh SL, Strain EC, Abreu ME, Bigelow GE. Enadoline, a selective kappa opioid agonist: comparison with butorphanol and hydromorphone in humans. Psychopharmacology (Berl). 2001 Sep;157(2):151-62. — View Citation

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