Improvement of Depression With Use of ATP
- Disease/Condition
- Depression
- Drug/Device/Intervention
- ATP Group
- Study type
- Interventional
- Intervention type
- drug
- Primary sponsor
- Nanfang Hospital, Southern Medical University
- Location
- Guangzhou, China
- Phase
- N/A
- Start date
- Mar 04, 2024
- End date
- Dec 31, 2026
- Enrollment
- 120 participants
HAMD-24
This clinical study is a randomized, double-blind, placebo-controlled trial with an
 intervention period of 4 weeks. Participants will be patients with moderate to severe
 depression who meet the inclusion criteria during the screening period. After recruitment
 written informed consent form will be signed and the baseline evaluation will be done then
 the treatment period follows. The subjects will be randomly assigned to a control group
 (escitalopram plus normal saline(NA)) and an ATP group (escitalopram plus adenosine disodium
 triphosphate(ATP)) in a 1:1 ratio for treatment, with a total number of 120 recruited
 patients. Assessment will be carried out as an analysis of changes in Hamilton Depression
 Scale(HAMD-24), cognitive function test, brain functional network, inflammatory markers, and
 other indicators in the first, second, and fourth week of intervention which will evaluate
 the effectiveness of ATP in improving moderate to severe depression preliminarily.
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT06266715
- Type
- Non-Device Trial
Access comprehensive clinical trial information for NCT06266715 through Pure Global AI's free database. This phase not specified trial is sponsored by Nanfang Hospital, Southern Medical University and is currently Recruiting. The study focuses on Depression. Target enrollment is 120 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.