Supersaturated Hydrogen-Rich Water for Outpatients With Persistent Excess Weight
NCT07410065 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 120
Last updated 2026-02-13
Summary
The Supersaturated Hydrogen-Rich Water for Outpatients with Persistent Excess Weight (HOPE) study is a Phase III, multicenter, randomized, double-blind, placebo-controlled study designed to evaluate the efficacy and safety of daily consumption of supersaturated hydrogen-rich water in adults with persistent excess body weight. The trial investigates whether sustained exposure to molecular hydrogen can favorably influence body composition and key metabolic outcomes compared with a placebo water lacking dissolved hydrogen. By enrolling outpatients across multiple centers and applying rigorous blinding and randomization procedures, HOPE aims to generate high-quality clinical evidence on the potential role of hydrogen-rich water as a non-pharmacological, adjunctive strategy for weight management and metabolic health.
Conditions
Interventions
- DIETARY_SUPPLEMENT
-
Hydrogen-rich water
Hydrogen-rich water (1.0 L per day)
- DIETARY_SUPPLEMENT
-
Control
Hydrogen-free water (1.0 L per day)
Sponsors & Collaborators
-
Center for Health Sciences, Serbia
lead OTHER
Principal Investigators
-
Nikola Todorovic, PhD · Center for Mitochondrial Medicine
Study Design
- Allocation
- RANDOMIZED
- Purpose
- SUPPORTIVE_CARE
- Masking
- QUADRUPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2026-04-15
- Primary Completion
- 2027-01-15
- Completion
- 2027-02-15
Countries
- Serbia
Study Locations
More Related Trials
-
A Study of Enicepatide (CT-388) in Participants With Obesity or Overweight With at Least One Weight-Related Comorbidity
NCT06525935 ·Status: COMPLETED ·Phase: PHASE2
-
Long-term Efficacy and Safety of HRS-7535 Tablets in Obese Subjects
NCT06671821 ·Status: COMPLETED ·Phase: PHASE2
-
Efficacy and Safety of Attapulgite in Patients With Obesity: An Exploratory Clinical Trial
NCT07103382 ·Status: RECRUITING ·Phase: NA
-
Efficacy and Safety of HRS-7535 Tablets in Obese Subjects .
NCT06250946 ·Status: COMPLETED ·Phase: PHASE2
-
A Trial Within Cohort Feasibility Study Design Comparing Standard of Care Versus Weight Loss (Achieved Through Tirzepatide) for Obesity-related Hypertension in Young Adults
NCT07364175 ·Status: RECRUITING ·Phase: NA
-
A Study Evaluating the Effect of Daily Oral RO7795081 in Participants With Obesity or Overweight With at Least One Weight-Related Comorbidity
NCT07081958 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE2
-
A Study to Compare Two Different Forms of PF-07081532 in Adults Who Are Overweight or Obese
NCT05677867 ·Status: COMPLETED ·Phase: PHASE1
-
Safety and Efficacy of Sodium Pentaborate Pentahydrate in People With Overweight and Obesity
NCT05741606 ·Status: UNKNOWN ·Phase: PHASE1/PHASE2
-
Relative Bioavailability of First vs Second-Generation Formulations of HRS9531 Tablets in Obese or Overweight Subjects
NCT07150962 ·Status: RECRUITING ·Phase: PHASE1
-
A Study to Test the Effect of Survodutide (BI 456906) on Cardiovascular Safety in People With Overweight or Obesity (SYNCHRONIZE™ - CVOT)
NCT06077864 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE3
-
A Study to Test Whether Survodutide (BI 456906) Helps Chinese People Living With Overweight or Obesity to Lose Weight
NCT06214741 ·Status: COMPLETED ·Phase: PHASE3
-
A Study to Test Whether Survodutide (BI 456906) Helps People Living With Overweight or Obesity Who do Not Have Diabetes to Lose Weight
NCT06066515 ·Status: COMPLETED ·Phase: PHASE3
-
A Study in People With Overweight or Obesity to Compare How 2 Different Formulations of Survodutide Are Taken up by the Body
NCT07407348 ·Status: RECRUITING ·Phase: PHASE1
-
To Compare the Efficacy and Safety of HRS9531 and Placebo in Subjects With Overweight or Obese
NCT06396429 ·Status: COMPLETED ·Phase: PHASE3
-
Evaluating Anti-Obesity Medications 6 Months After Metabolic Surgery
NCT07163650 ·Status: RECRUITING ·Phase: PHASE4
-
A Phase 2b Study to Examine the Safety and Efficacy of Once-Weekly MET097 in Adults With Obesity or Overweight
NCT06712836 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE2
-
A Study of HS-20094 in Chinese Adults with Overweight or Obesity
NCT06839664 ·Status: RECRUITING ·Phase: PHASE3
-
Efficacy and Safety of MET097 Once-Weekly in People With Overweight or Obesity
NCT07311850 ·Status: RECRUITING ·Phase: PHASE3
-
DBRPC Study to Evaluate the Efficacy and Safety of IQP-AE-103 in Overweight and Moderately Obese Subjects
NCT04086797 ·Status: COMPLETED ·Phase: NA
-
Study of Tesomet With Open-label Extension in Subjects With Hypothalamic Obesity (HO)
NCT05147415 ·Status: WITHDRAWN ·Phase: PHASE2
-
A Study to Evaluate the Efficacy and Safety of DA-302168S Tablets in Overweight/Obese Subjects
NCT06953063 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE2
-
A Study Evulating DA-302168S Tablets in Overweight/Obese Subjects
NCT06541730 ·Status: COMPLETED ·Phase: PHASE1
-
Prediction of the SURPASS-CVOT Cardiovascular Outcome Trial in Healthcare Claims Data
NCT07088718 ·Status: COMPLETED
-
A Study to Test Whether BI 456906 (Survodutide) Influences the Amount of Bupropion, Caffeine and Midazolam in the Blood in People With Overweight or Obesity
NCT06564441 ·Status: COMPLETED ·Phase: PHASE1
-
Benefit and Tolerability of IQP-AE-103 in Weight Loss
NCT03058367 ·Status: COMPLETED ·Phase: NA