Carbon Dioxide Laser vs. Electrocoagulation for the Therapy of Condyloma

  • End date
    Dec 2, 2024
  • participants needed
  • sponsor
    Zydolab - Institute of Cytology and Immune Cytochemistry
Updated on 2 August 2021
carbon dioxide
laser ablation


In a randomized clinical trial of 114 women undergoing Treatment for condyloma acuminata, two surgical methods, the carbon dioxide laser Ablation and the excision by electrocoagulation, will be compared. The primary outcome of the study is the cosmetic result judged by the Patient 6 weeks after Treatment using a 11-step visual analogue scale (VAS), secondary outcomes are intervention time, operative complications, subjects and users satisfaction, postoperative pain and recurrence of genital warts.

Condition Condyloma acuminatum, Verruca vulgaris, Genital Warts, Warts, condyloma, venereal warts
Treatment Carbon dioxide Laser ablation, Electrocoagulation, Electrocoagulation
Clinical Study IdentifierNCT02520986
SponsorZydolab - Institute of Cytology and Immune Cytochemistry
Last Modified on2 August 2021


Yes No Not Sure

Inclusion Criteria

informed consent
women with anogenital affection of condyloma acuminata

Exclusion Criteria

significant language barrier
unwillingness to participate
the use of blood thinner or known coagulation disorder
the use of immunosuppressive medicament
malignant diseases
local therapy within 8 weeks before Treatment
wound healing disorder
Clear my responses

How to participate?

Step 1 Connect with a site
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

You are contacting

Investigator Avatar

Primary Contact


Preferred Language
Other Language
Please verify that you are not a bot.

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

Learn more

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

Similar trials to consider


Browse trials for

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer

user name

Added by • 



Reply by • Private

Lorem ipsum dolor sit amet consectetur, adipisicing elit. Ipsa vel nobis alias. Quae eveniet velit voluptate quo doloribus maxime et dicta in sequi, corporis quod. Ea, dolor eius? Dolore, vel!

  The passcode will expire in None.

No annotations made yet

Add a private note
  • abc Select a piece of text from the left.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.
Add a private note