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Microbotox injection versus oral isotretinoin tablets in treating patients with oily skin and acne-A comparative study.

A study to evaluate the efficacy and safety of microbotox versus oral isotretinoin therapy in treating seborrhea and acne-A randomized controlled pilot study. - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/071250
Enrollment
30
Registered
2024-07-25
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Health Condition 1: L700- Acne vulgaris

Interventions

Intervention1: Microbotox injection: Diluted botulinum toxin injection given into the skin of the face. Control Intervention1: Isotretinoin tablets: Oral isotretinoin tablets at the dose of 20mg daily

Sponsors

Aishwarya Satyanarayana
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients above the age of 18 years, with seborrhea which meets the criteria as per skin oiliness and acne which requires isotretinoin therapy. Patients who are willing to provide informed consent will be considered for participation in the study.

Exclusion criteria

Exclusion criteria: Patients with active infection at injection site, neuromuscular disorders, known hypersensitivity to any ingredient of the injection. Pregnant and lactating women. Patients on oral steroid therapy, anticoagulant therapy, systemic retinoid intake in the previous six months. Patients with unrealistic expectations.

Design outcomes

Primary

MeasureTime frame
Reduction in the subjective seborrhea severity graded on a scale of 1 to 10, 1 being mild and 10 being severe from baseline to 3 months.Timepoint: Reduction in the subjective seborrhea severity at baseline, 4weeks, 8weeks and 12weeks.

Secondary

MeasureTime frame
Reduction in the Comprehensive Acne Severity Score from baseline to 3 months.Timepoint: Baseline at 0weeks, follow up visits at 4,8,12 weeks.

Countries

India

Contacts

Public ContactAishwarya Satyanarayana

Bangalore medical college and research institute, Bangalore

eshwari.nithyanand@gmail.com9845935375

Outcome results

None listed

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