Prospective randomised controlled study on tumescent local anesthesia for Mohs Micrographic Surgery ( MMS) compared to conventional anesteshia with lidocaine/ epinephrine 1 %

Prospective randomised controlled study on tumescent local anesthesia for Mohs Micrographic Surgery ( MMS) compared to conventional anesteshia with lidocaine/ epinephrine 1 % - Tumescent local anesteshia for Mohs Micrographic surgery.

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON34466

Enrollment

Registered

2010-06-17

Start date

2010-10-18

Completion date

Unknown

Last updated

2024-05-06

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

Conditions

Painsensation

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients with a basal cell carcinoma on the scalp, the nose, or the forehead, wich will be treated with Mohs micrographic surgery.

Exclusion criteria

Exclusion criteria: Allergy for lidocaine/epinephrine 1% or substances in the tumescent.

Design outcomes

Primary

Measure	Time frame
Registration of the pain perception during anesthesia. Registration of the pain during the operation . Registration of the pain postoperative .	—

Secondary

Measure	Time frame
The duration of the anesthetic effects. The vasoconstrictive effects of the TLA.	—

Countries

Netherlands

Outcome results