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Patients suffering from androgenetic alopecia are to be treated with rosemary oil along with minoxidil 5 percent in one group, minoxidil 5 percent in another group and rosemary oil alone to compare the effect of the treatments in different groups in respect to reduction in hair loss.

Comparative evaluation of Effectiveness of Minoxidil 5 percent with Rosemary oil, Minoxidil 5 percent and Rosemary oil alone in the treatment of Androgenetic alopecia. - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/06/089089
Enrollment
60
Registered
2025-06-18
Start date
Unknown
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Health Condition 1: L00-L08- Infections of the skin and subcutaneous tissue

Interventions

Intervention1: ROSEMARY OIL: Rosemary oil inhibits 5alpha reductase to be intervened for one year duration. Control Intervention1: MINOXIDIL 5%: Approved for androgewnetic alopecia by FDA.

Sponsors

Dr Natasha Biswas
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Male patients between 18 yrs to 50 yrs of age. 2)Patients with AGA grade I-V of modified Hamilton Norwood Scale 3)Willing to give a written consent

Exclusion criteria

Exclusion criteria: 1)Patients taking Finasteride or any other medications for the treatment of AGA 2)Any dermatological diseases of scalp 3)History of use of Platelet rich plasma therapy in the past 4)Patients with existing neuro-psychiatric disorders & any other associated pre-existing medical illness like autoimmune conditions, thyroid disorder, iron deficiency anaemia, undergoing radiation therapy, malnutrition.

Design outcomes

Primary

MeasureTime frame
To study and compare decrease in hair loss in all the 3 groups. Timepoint: To study and compare decrease in hair loss in all the 3 groups.

Secondary

MeasureTime frame
1)To compare increase in hair growth in all 3 groups 2)To compare significant improvement in the duration of treatment required in all 3 groups 3)To compare scaling, dandruff, scalp itchingTimepoint: 15 days- for complaints 3 months- follow up 6 months- follow up 9 months- follow up 12 months- follow up

Countries

India

Contacts

Public ContactNatasha Biswas

SCB Medical college and hospital, Cuttack

drrashmita15@gmail.com9437268984

Outcome results

None listed

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