Study on the Effectiveness of Nimson Boroneem Talcum Powder in Reducing Sweat and Body Odor.

A Prospective Single-Arm Open Label Single Centre Study to Evaluate The Effectiveness Of Nimson Boroneem Talcum Powder In Reducing Sweat And Body Odor - Nil

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/11/076337

Enrollment

Registered

2024-11-06

Start date

Unknown

Completion date

Unknown

Last updated

2024-11-11

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

Conditions

Health Condition 1: R61- Generalized hyperhidrosis Health Condition 2: R61- Generalized hyperhidrosis

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1. Adults aged 18-60 years. 2. Experiencing excessive sweating and body odor. 3. Willing to provide informed consent.

Exclusion criteria

Exclusion criteria: 1. Known allergies to talcum powder or its components. 2. Skin conditions that may interfere with the study. 3. Participation in another clinical trial within the last 30 days

Design outcomes

Primary

Measure	Time frame
Reduction in skin irritation and excessive sweating, measured by patient-reported outcomes and clinical assessment at baseline, week 2, week 4, week 6, and week 8.Timepoint: Day 1, Day 15, Day 30, Day 45 and Day 60	—

Secondary

Measure	Time frame
Safety assessed by the incidence of adverse events throughout the study. Likert scale measured patient satisfaction at week 8.Timepoint: Day 1, Day 15, Day 30, Day 45 and Day 60	—

Countries

India

Contacts

Public ContactMs Arpita Malgi

Samahitha Research Solutions

satyalm@samahitha.com9739001749

Outcome results