This is a study conducted among patients with lump in the upper or lower jaw who will undergo surgery for its removal and repair using thin bone in the leg by planning either by computer or by surgeon without help of computer and to compare the scan report.

Comparison of radiological outcomes of virtual surgical planning versus conventional surgical planning in maxillofacial reconstruction using free fibula osseocutaneous flap: a non-randomised controlled trial - Nill

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/02/102712

Enrollment

Registered

2026-02-02

Start date

Unknown

Completion date

Unknown

Last updated

2026-03-02

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

Conditions

Health Condition 1: C069- Malignant neoplasm of mouth, unspecified

Interventions

Intervention1: Maxillofacial reconstruction using free fibula osseocutaneous flap by virtual surgical planning.: Patients with benign and malignant diseases of maxilla or mandible will undergo reconst

Eligibility

Inclusion criteria

Inclusion criteria: Patients with benign or malignant disease of mandible or maxilla who will require free fibular osseocutaneous flap. Consenting to participate in the study and not a part of any other trial or study.

Exclusion criteria

Exclusion criteria: Patients with peripheral vascular disease. Patients who are unfit for surgery (uncontrolled diabetes, severely immunocompromised disease). Evidence of tumour recurrence with bone invasion. Not willing for consent

Design outcomes

Primary

Measure	Time frame
Bony union evaluated by NCCT head and neckTimepoint: 6 months postoperatively	—

Secondary

Measure	Time frame
Intraoperative time and flap ischemia timeTimepoint: In operation theatre;Postoperative complications including returning to operating room, major bleeding events, venous thromboembolism, flap vascular compromise, flap necrosis, wound dehiscence, infection, bone exposure and orocutaneous fisstula will be assessed.Timepoint: Immediate postoperative period, at 3 and 6 months postoperatively.;Quality of life assessed using EORTC QLQ H&N 35 questionnaireTimepoint: 6 months postoperatively;Mandibular asymmetry and mandibular angle by NCCT headTimepoint: 6 months postoperatively	—

Measure

Time frame

Intraoperative time and flap ischemia timeTimepoint: In operation theatre;Postoperative complications including returning to operating room, major bleeding events, venous thromboembolism, flap vascular compromise, flap necrosis, wound dehiscence, infection, bone exposure and orocutaneous fisstula will be assessed.Timepoint: Immediate postoperative period, at 3 and 6 months postoperatively.;Quality of life assessed using EORTC QLQ H&N 35 questionnaireTimepoint: 6 months postoperatively;Mandibular asymmetry and mandibular angle by NCCT headTimepoint: 6 months postoperatively

—

Countries

India

Contacts

Public ContactDr Ajeena M M

All India Institute of Medical Sciences, Patna

drsveena@aiimspatna.org9905755111

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026