Skip to content

Comparison of the therapeutic effect of cryotherapy, CO2 laser and conventional surgery in the treatment of mucocele

Comparison of the therapeutic effect of cryotherapy, CO2 laser and conventional surgery in the treatment of mucocele

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240805062659N1
Enrollment
45
Registered
2024-09-28
Start date
2024-10-22
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

Mucocele. Mucocele of salivary gland

Interventions

Intervention 1: Control group: Using scalpel by placing an incision circumferentially Lesion will be resected from the base. Intermittent sutures will be placed, and suture removal will be done after

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
10 Years to No maximum

Inclusion criteria

Inclusion criteria: Age above 10 years with intraoral mucoceles in the lower labial mucosa without infection Size lower than 2 cm

Exclusion criteria

Exclusion criteria: Patients with cold intolerance Having Reynaud's disease or with a history of diabetes and gross infections Smoker Patients with any problem that conflict with wound healing such as cryoglobulinemia Cold urticaria or undergoing hemodialysis or immunosuppressive therapy

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: 1 and 3 weeks after surgery. Method of measurement: Postoperative pain is assessed using a 10-point visual analog scale (VAS), from 0 for "no pain" to 10 for "worst possible pain". The patients will be questioned for the pain at standard intervals, i.e., 1st, 3rd postoperative day, 1st and 3rd postoperative week. Four categories of scoring will be used:0 = No pain – There will be no need for the patient to take analgesics1–3 = Mild pain – When patients either tolerated or taken one analgesic tablet4–7 = Moderate pain – When the patient felt definite pain and needed more than one tablet8–10 = Severe pain – When the patient felt severe pain and either reported back or took stronger analgesics.;Wound Healing. Timepoint: 1 and 3 weeks after surgery. Method of measurement: Early Wound Healing Assessment with EHSEHS assessment was composed of the parameters clinical signs of re-epithelization (CSR), haemostasis (CSH) and inflammation (CSI) (31).CSR = 0 points: visible distance between incision margins, 3 points: contact between incision margins, 6 points: merged incision margins;CSH = 0 points: bleeding at the incision margins, 1 point: presence of fibrin on the incision margins, 2 points: absence of fibrin on the incision margins;CSI = 0 points: redness involving >50% of the incision length and/or pronounced swelling, 1 point: redness involving <50% of the incision length, 2 points: absence of redness along the incision length.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSara Maroufi

Shiraz University of Medical Sciences

sara.maroufi19@gmail.com+98 71 3626 3193

Outcome results

None listed

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