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Comparing two different instruments used for intraoral incision in oral major surgical procedures - A clinical trial

Comparison of the effectiveness of stainless-steel scalpel and electrocautery in oral mucoperiosteal incision wound outcome, in oral major surgical procedure ? A clinical trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/093303
Enrollment
26
Registered
2025-08-20
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Electrocautery and scalpel: Patients will be selected randomly into two groups, both of which will undergo major oral surgical procedures. In the first group oral mucosal incision will

Sponsors

Saraswathi Lakshmi Yatam
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients who require oral vestibular incision for management and correction of any facial deficits. Orthognathic surgical procedures which require intra-oral vestibular incision. Oral and maxillofacial pathologies involving only hard tissue which require intra-oral mucosal incisions. Patient more than 18 years old. Healthy patients, ASA I & II.

Exclusion criteria

Exclusion criteria: Medically compromised patients such as patients with history of bleeding disorder, collagen disorder, diabetes, hypertension, ASA III, IV, V, VI. Presence of bone fractures in the region. Presence of pathology along the line of incision. Presence of intra oral laceration/wound in the site of incision. Presence of ecchymosis in the site of incision.

Design outcomes

Primary

MeasureTime frame
To compare the efficacy of electrocautery and stainless-steel scalpel incisions in oral surgical procedures in terms of time taken for incision, healing efficacy, blood loss, post operative pain assessment, scar formation.Timepoint: Time taken for incision and bleeding measured at baseline during surgery. Post-operative pain, healing efficacy measured within 2 weeks after surgery. Mucosal scarring index measured within 12 weeks

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactSaraswathi Lakshmi Yatam

Amrita Vishwa Vidyapeetham Amrita School of Dentistry

dr.ravi.omfs@gmail.com07708160312

Outcome results

None listed

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