Actively Recruiting

Early Phase 1
Age: 18Years - 55Years
All Genders
Healthy Volunteers
NCT05008146

Imaging CRF X NOP Interactions in CUD

Led by Rajesh Narendran · Updated on 2025-06-05

80

Participants Needed

1

Research Sites

400 weeks

Total Duration

On this page

Sponsors

R

Rajesh Narendran

Lead Sponsor

N

National Institute on Drug Abuse (NIDA)

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study uses \[11C\]NOP-1A positron emission tomography (PET) and a hydrocortisone challenge to image the interaction between nociceptive opioid peptide (NOP) receptors and cortisol/corticotrophin releasing factor (CRF) in subjects with cocaine use disorders (CUD) and matched healthy controls (HC). It will also examine whether alterations in CRF x NOP interactions predict relapse in subjects with CUD.

CONDITIONS

Official Title

Imaging CRF X NOP Interactions in CUD

Who Can Participate

Age: 18Years - 55Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Males or females between 18 and 55 years old
  • For CUD group: Fulfill DSM-5 criteria for cocaine use disorder
  • For healthy controls: No present or past DSM-5 disorders except nicotine dependence
  • No current abuse of opiates, sedative-hypnotics, amphetamines, MDMA, moderate to severe alcohol or cannabis use
  • Not currently on prescription medical or psychotropic medications
  • No current or past severe medical, endocrine, or neurological illnesses
  • No metallic objects in the body contraindicated for MRI
  • No significant radioactivity exposure in past year exceeding guidelines
  • Not currently pregnant or breastfeeding
Not Eligible

You will not qualify if you...

  • Presence of other current DSM-5 psychiatric or addictive disorders besides cocaine use disorder
  • Current abuse within six months of opiates, sedative-hypnotics, amphetamines, MDMA, moderate to severe alcohol or cannabis use
  • Use of prescription medical or psychotropic medications
  • Severe medical, endocrine, or neurological illnesses including glaucoma, seizure disorders, hypertension, hypercholesterolemia
  • Pregnancy or breastfeeding
  • History of significant radioactivity exposure exceeding guidelines
  • Presence of metallic objects contraindicated for MRI

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Pittsburgh

Pittsburgh, Pennsylvania, United States, 15213

Actively Recruiting

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Research Team

R

Rajesh Narendran, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

BASIC_SCIENCE

Number of Arms

1

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