Pure Global

Whole-body Hyperthermia for Depression - Trial NCT06323785

Access comprehensive clinical trial information for NCT06323785 through Pure Global AI's free database. This phase not specified trial is sponsored by University of Zurich and is currently Recruiting. The study focuses on Major Depressive Disorder. Target enrollment is 30 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

Free Database
Powered by Pure Global AI
840K+ Trials
Device Trial
NCT06323785
Recruiting
Device Trial
device
Trial Details
ClinicalTrials.gov โ€ข NCT06323785
View on ClinicalTrials.gov
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Whole-body Hyperthermia for Depression
Randomised Sham-controlled Trial of Whole-body Hyperthermia for Depression

Study Focus

Major Depressive Disorder

Active whole-body hyperthermia

Interventional

device

Sponsor & Location

University of Zurich

Zurich, Switzerland

Timeline & Enrollment

N/A

Apr 30, 2024

Mar 01, 2026

30 participants

Primary Outcome

Hamilton Rating Scale for Depression (HAMD-17; minimum: 0, maximum: 68, higher scores indicate higher depression)

Summary

The goal of this clinical trial is to test the efficacy of whole-body hyperthermia in major
 depression. The main question it aims to answer is:
 
 โ€ข Does whole-body hyperthermia alleviate symptoms of depression?
 
 Participants will be randomised to sham or active whole-body hyperthermia. The study will
 last 6 weeks during which five visits will take place. Depression will be measured repeatedly
 and biological mechanisms will be investigated.

ICD-10 Classifications

Recurrent depressive disorder
Recurrent depressive disorder, unspecified
Depressive conduct disorder
Other recurrent depressive disorders
Recurrent depressive disorder, current episode moderate

Data Source

ClinicalTrials.gov

NCT06323785

Device Trial