| 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
|
|
|
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
|
|
|
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. |