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RecruitingNCT06976424Updated Jul 3, 2025

Comparison of a Face Cream Plus a Laser Procedure and Face Cream Alone in Treatment of Excessive Face Hairs in Female

A Phase 4 interventional study of Eflornithine Topical and Instense pulsed light in Hirsuitism, sponsored by Khyber Teaching Hospital. Recruiting at 3 sites in Pakistan. Open to female participants aged 18 Years to 45 Years. Per ClinicalTrials.gov, last updated 2025-07-03.

Sponsored by Khyber Teaching Hospital · Phase 4, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Dec 2025, 10 months ago, but the record still lists the study as recruiting.
Phase
Phase 4
Study type
Interventional
Enrollment
122
Allocation
Randomized
Ages
18 Years to 45 Years
Sex
Female
01

Study summary

The study compares the effects of a cream alone and a combined effect of cream and laser for the treatment of excessive facial hairs in women .

Read the detailed description

Hirsuitism refers to excessive terminal hairs in females, following a distribution pattern typically associated with male. It is associated with either increase response of hair follicles to androgen or either increase level of circulating androgens.The treatment options available are topical creams like eflornithine and laser treatments for hair removal. This study aims to conduct the comparison of a eflornithine cream and intense pulsed light laser versus eflornithine cream alone for the treatment of excessive facial hairs.

02

Conditions studied

  • Hirsuitism

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Keywords

  • Hirsuitism
  • IPL
  • Eflornithine
03

In context

Hirsutism

41 studies on the registry are indexed under Hirsutism; 8 are open to participants now.

This study's planned enrollment of 122 is above the median of 43 across 26 interventional studies indexed under Hirsutism.

Browse Hirsutism studies →

Lead sponsor

Khyber Teaching Hospital is the lead sponsor of 29 studies on the registry; 19 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 45 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

Gender (Female) Age between 18-45 Years Women with hirsutism as mentioned in the operational definition

Exclusion criteria

Exclusion Criteria:

Pregnant women Women with severe acne Women with immunodeficiency

05

Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
122 participants (estimated)

Study arms

  • Experimental
    GroupA

    This group is treated with combination of eflornithine cream and intense pulsed light for a period of three month.

    Radiation: Instense pulsed light · Drug: Eflornithine Topical

  • Experimental
    Group B

    This group is treated with eflornithine cream twice daily only for a period of three month

    Drug: Eflornithine Topical

Interventions

  • DrugEflornithine Topical

    Eflornithine cream will be applied to the face of group B female patients

    Also known as: Eflornithine cream

  • RadiationInstense pulsed light

    Intense pulse light will be applied to the face of patient of Group A on areas having increase hair. Patient will be called for a followup every month for next session.

  • DrugEflornithine Topical

    Eflornithine will be given to group A patient along with intense pulsed light and results will be compared to group B who recieved only Eflornithine cream

06

What researchers measure

Primary outcomes

  1. Efficacy of treatment

    Efficacy of treatment is defined as complete clearance of excessive hairs assesed on the basis of 4- level scale ranging 0 to 3 after 3 months of administration of the treatment in both groups. Clear is grade 3 Marked improvement is grade2 Improved is grade1 No improvement is grade 0

    Time frame: 3 months

07

Study locations

3 of 3 sites recruiting
08

References and documents

Individual participant data

Plan to share: No — Because the confedentiality of the patient would be breached.

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Jul 2025; primary completion for Dec 2025, 5 months later.

How these figures are worked out, and which studies are left out of them.

Registered
May 9, 2025
First posted
May 16, 2025
StartEst.
Jul 15, 2025
Primary completionEst.
Dec 31, 2025
CompletionEst.
Dec 31, 2025
Last update
Jul 3, 2025
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 3, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06976424
Lead sponsor
Khyber Teaching Hospital
Responsible party
Umaima Nazar (Doctor, Khyber Teaching Hospital) — Principal investigator
First posted
May 16, 2025
Start date
Jul 15, 2025 (estimated)
Primary completion
Dec 31, 2025 (estimated)
Completion
Dec 31, 2025 (estimated)
Last update
Jul 3, 2025

Study contacts

Umaima Nazar, MBBS
Contact
umaimanazar123@gmail.com
+923355869079 ext. +923355869079

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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