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CTRI Number  CTRI/2025/07/091115 [Registered on: 18/07/2025] Trial Registered Prospectively
Last Modified On: 20/02/2026
Post Graduate Thesis  No 
Type of Trial  Interventional 
Type of Study   Nutraceutical 
Study Design  Randomized, Parallel Group, Placebo Controlled Trial 
Public Title of Study   A Study to Test a Nutraceutical Supplement for Supporting Thyroid Function in Adults with Hypothyroidism 
Scientific Title of Study   A Randomized placebo controlled clinical study to evaluate the efficacy of a plant based Nutraceutical formulation in patients with hypothyroidism 
Trial Acronym  NIL 
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Dr Ragavendra Pandilwar 
Designation  Associate Professor 
Affiliation  Dr. G. D. POL Foundation Y. M. T. Ayurvedic Medical College and Hospital 
Address  Dr.G.D.POL Foundation, Y.M.T. Ayurvedic Medical college and Hospital Institutional Area , sector 4 Kharghar, Navi Mumbai 410210
Institutional Area ,sector 4 Kharghar Navi Mumbai 410210
Raigarh
MAHARASHTRA
410210
India 
Phone  9699365567  
Fax    
Email  raghavendra.pandilwar@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Shefali Thakkar 
Designation  Head- Research and Product Development 
Affiliation  Arelang Naturals Pvt. Ltd. 
Address  Department of Research and Product Development 28, Raghuvanshi Mills Compound, Senapati Bapat Marg, Lower Parel, Mumbai 400013
28, Raghuvanshi Mills Compound, Senapati Bapat Marg, Lower Parel, Mumbai 400013
Mumbai
MAHARASHTRA
400013
India 
Phone  8879350005  
Fax    
Email  shefali@arelang.com  
 
Details of Contact Person
Public Query
 
Name  Shefali Thakkar 
Designation  Head- Research and Product Development 
Affiliation  Arelang Naturals Pvt. Ltd. 
Address  Department of Research and Product Development, 28, Raghuvanshi Mills Compound, Senapati Bapat Marg, Lower Parel, Mumbai 400013
28, Raghuvanshi Mills Compound, Senapati Bapat Marg, Lower Parel, Mumbai 400013
Mumbai
MAHARASHTRA
400013
India 
Phone  8879350005  
Fax    
Email  shefali@arelang.com  
 
Source of Monetary or Material Support  
Arelang Naturals Pvt. Ltd. 28, Raghuvanshi Mills Compound Senapati Bapat Marg Lower Parel Mumbai 400013 
 
Primary Sponsor  
Name  Arelang Naturals Private Limited 
Address  28, Raghuvanshi Mills Compound Senapati Bapat Marg Lower Parel Mumbai 400013 
Type of Sponsor  Other [Private Nutraceutical Company] 
 
Details of Secondary Sponsor  
Name  Address 
NIL  NIL 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 1  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Dr Raghavendra Pandilwar  Dr. G. D. POL Foundation Y. M. T. Ayurvedic Medical College and Hospital  Institutional Area Sector 4 Kharghar Navi Mumbai 410210
Raigarh
MAHARASHTRA 
9699365567

raghavendra.pandilwar@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Institute Ethics Committee for Research Dr.G.D.POL FOUNDATION Y.M.T.Ayurvedic Medical college and Hospital PG INSTITUTE  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: E039||Hypothyroidism, unspecified,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Comparator Agent  Placebo  Group A will consume Placebo alongwith Thyroxine empty stomach every morning 
Intervention  ThyPhy for Balance  Group B will consume ThyPhy for Balance alongwith Thyroxine medication empty stomach every morning 
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  65.00 Year(s)
Gender  Both 
Details  Clinically diagnosed with overt hypothyroidism within the past 6 months.
On dose of thyroxine therapy for at least 1 week prior to screening.
Able and willing to provide written informed consent.
Willing to comply with study procedures follow up visits and sample collection.
Agree to refrain from taking any new supplements or herbal products targeting thyroid during the trial.
Negative pregnancy test for women of childbearing potential and commitment to use contraception during the study.
 
 
ExclusionCriteria 
Details  Pregnant or Lactating women.
History of active hyperthyroidism, thyroid cancer or thyroidectomy.
Presence of severe comorbidities like chronic kidney disease, liver dysfunction, cardiovascular disease.
Use of other investigational drug or agent in last 30 days.
Known allergy or hypersensitivity to herbal ingredients.
Diagnosed with psychiatric or cognitive disorder that may affect informed consent or compliance.
Individual with uncontrolled diabetes mellitus.
History of substance abuse or alcohol in past 6 months.
Any other concern deemed by the investigator to interfere with the participants or study outcomes. 
 
Method of Generating Random Sequence   Computer generated randomization 
Method of Concealment   Other 
Blinding/Masking   Participant Blinded 
Primary Outcome  
Outcome  TimePoints 
Change in serum TSH and Free T4 levels from baseline to Week 12 in intervention group  day zero and day ninety 
 
Secondary Outcome  
Outcome  TimePoints 
Change in the subjective criteria which includes: Weight gain, Lethargy & Fatigue, Constipation, Puffiness of Face, Amenorrhea, Hair loss, Skin Dryness, Hoarseness of voice, Cold Intolerance, Slowed Movement, Difficulty concentration and poor memory  day zero to day 15 to day 30 to day 45 to day 60 to day 75 to day 90 
Stabilization or reduction of Thyroxine dose  day zero to day 90 
 
Target Sample Size   Total Sample Size="150"
Sample Size from India="150" 
Final Enrollment numbers achieved (Total)= "0"
Final Enrollment numbers achieved (India)="150" 
Phase of Trial   Phase 2 
Date of First Enrollment (India)   01/08/2025 
Date of Study Completion (India) 05/02/2026 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Date Missing 
Estimated Duration of Trial   Years="0"
Months="6"
Days="0" 
Recruitment Status of Trial (Global)
Modification(s)  
Not Applicable 
Recruitment Status of Trial (India)  Completed 
Publication Details   N/A 
Individual Participant Data (IPD) Sharing Statement

Will individual participant data (IPD) be shared publicly (including data dictionaries)?  

Response - NO
Brief Summary
Modification(s)  

Primary hypothyroidism is a chronic endocrine disorder in which many patients continue to experience symptoms such as fatigue, lethargy, sleep disturbances, cognitive complaints, and reduced functional capacity despite receiving standard thyroxine therapy. These persistent symptoms may significantly affect quality of life and daily functioning, indicating a need for safe adjunctive interventions that can support overall clinical outcomes.

Plant-derived bioactive compounds have been investigated for their potential role in supporting thyroid physiology and systemic metabolic balance; however, controlled clinical evidence evaluating such formulations as adjuncts to standard therapy remains limited. Evaluating both efficacy and safety in a randomized, placebo-controlled setting was therefore considered necessary.

This randomized, single-blind, placebo-controlled, parallel-group clinical study evaluated the efficacy and safety of ThyPhy for Balance as an adjunct to levothyroxine therapy in adults with primary hypothyroidism over 12 weeks. A total of 150 participants were randomized (75 per group), and all completed the study.

Primary outcome:

Both groups demonstrated increases in Free T3 and Free T4 (p<0.001). Intergroup comparison at Week 12 showed significantly higher Free T4 (p=0.038) and significantly lower TSH (p=0.024) in the intervention group compared with placebo, while Free T3 did not differ significantly between groups (p=0.071). TSH reduction reached statistical significance only in the intervention group (p<0.001).

Secondary Outcome:

Intervention group showed statiscally significant improvement (p<0.001) in reduction of secondary outcomes including fatigue, lethargy, irritability, insomnia, dysphagia, forgetfulness, constipation.

Other symptoms such as swelling, weight gain, menstrual irregularity, and breathlessness improved in both groups.

Hashimoto’s subgroup:
In participants with elevated TPO antibodies, mean TSH increased over 12 weeks in both groups, consistent with the known variability of autoimmune hypothyroidism. Despite this biochemical variability, symptom improvement was observed in the intervention group.

Safety:
No adverse events, serious adverse events, or treatment discontinuations were reported.

Conclusion:
Adjunct administration of ThyPhy for Balance was associated with greater percentage improvement in several clinical symptoms and favorable changes in thyroid function parameters compared with placebo over 12 weeks, with good tolerability and safety.

 
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