Long-term Efficacy of Pramipexole in Anhedonic Depression

NCT05825235 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 55

Last updated 2026-04-28

No results posted yet for this study

Summary

The purpose of the study is to assess the long-term efficacy and safety of add-on pramipexole for treatment of patients with anhedonic depression.

Conditions

Interventions

DRUG

Pramipexole

6 months of treatment with add-on Pramipexole

Sponsors & Collaborators

  • Lund University

    collaborator OTHER
  • Region Skane

    lead OTHER

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-04-21
Primary Completion
2025-12-05
Completion
2025-12-05

Countries

  • Sweden

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05825235 on ClinicalTrials.gov