The Efficacy and Safety of Dezocine Pretreatment for Pain Relief in Acne Scar Treatment of Fractional CO2 Laser

  • STATUS
    Recruiting
  • participants needed
    105
  • sponsor
    Xijing Hospital
Updated on 10 January 2024

Summary

The Efficacy and Safety of Dezocine Pretreatment for Pain Relief in Acne Scar Treatment of Fractional CO2 Laser

Details
Condition Acne Atrophica
Age 18years - 60years
Treatment fractional CO2 laser, Dezocine
Clinical Study IdentifierNCT05861063
SponsorXijing Hospital
Last Modified on10 January 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

Age: 18-60 years old, regardless of gender
Clinical diagnosis of atrophic acne scars
Planning to undergo ultra-pulsed CO2 lattice laser therapy
The patient agrees to participate in this experiment and signs an informed consent form

Exclusion Criteria

Those who take sedative drugs for a long time
Patients with sleep apnea syndrome, previous history of hypertension, and blood pressure greater than 160/100mmHg
People with severe heart and lung diseases, liver and kidney diseases, psychosis, pregnancy, and communication disorders
Persons who are known to be allergic to the main drug or any of the excipients in Dezocine injection
Increased intracranial pressure or head injury
Acute and chronic alcoholism
People with hypotension, hypothyroidism, acute episodes of asthma, and epilepsy
\-
Clear my responses

How to participate?

Step 1 Connect with a study center
Message sent successfully.
We have submitted the information you provided to the research team at the location you chose. For your records, we have sent a copy of the message to your email address.
If you would like to be informed of other studies that may be of interest to you, you may sign up for Patient Notification Service.
Sign up

Send a message

Enter your contact details to connect with study team

Investigator Avatar

Primary Contact

First name*
Last name*
Email*
Phone number*
Other language

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

Loading...

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