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Constipation relieving herbal Syrup

â??To Evaluate the Safety and Tolerability of HCLX 031706 in Healthy Adult Volunteers: Randomized, Open Label, Two Arm, Clinical Studyâ??

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/02/017776
Enrollment
30
Registered
2019-02-22
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

None listed

Sponsors

The Himalaya Drug Company Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Young Healthy Adolescent male and female subjects. Aged between >=18 years to Subjects who can refrain or who are not on any other supplements for constipation Subjects willing to sign informed consent and follow the study procedure. Has not participated in any clinical study in the last one month.

Exclusion criteria

Exclusion criteria: Subjects with any clinical significant systemic illness. A known history or present condition of allergic response to products its components or to any of the ingredients in the test product Pre-existing systemic disease requiring long-term medications. Subjects treated with any laxatives 2 weeks prior to screening and are experiencing the laxative effect. Pregnant & nursing women.

Design outcomes

Secondary

MeasureTime frame
To assess overall compliance to the study interventionTimepoint: DAY 5 and DAY 7

Primary

MeasureTime frame
Normal values of all Laboratory parameters assessed before and after the intervention. To assess any Adverse events reported or observed during the study periodTimepoint: Screening/Day 1, Day 5 Day 7

Countries

India

Contacts

Public ContactDr Srikrishna H A

The Himalaya Drug Company Ltd

dr.palani@himalayawellness.com22199920

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026