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the incidence of nasotracheal intubation induced epistaxis in patients undergoing oromaxillofacial surgery

Comparison of nasal tip lifting and telescoping of tracheal tube on the incidence of nasotracheal intubation induced epistaxis in patients undergoing oromaxillofacial surgery: randomized comparative study - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/091971
Enrollment
43
Registered
2025-07-29
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Health Condition 1: R478- Other speech disturbances

Interventions

Intervention1: 1. To determine which technique reduces the incidence of nasotracheal intubation-induced epistaxis during various stages of anaesthesia ( at intubation , at extubation and during post o

Sponsors

Operation Theater
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All ASA physical status I to II adult patients 18 to 65 years of age scheduled to undergo elective oral and maxillofacial surgery requiring nasal intubation for general anesthesia Patients giving written informed consent will be taken

Exclusion criteria

Exclusion criteria: Patients with any nasal deformity, a history of massive or recurrent nasal bleeding, or abnormal coagulation function. Patients not giving consent

Design outcomes

Primary

MeasureTime frame
To determine which technique reduces the incidence of nasotracheal intubation-induced epistaxis during various stages of anaesthesia ( at intubation , at extubation and during post op recovery upto 24 hours ).Timepoint: To determine which technique reduces the incidence of nasotracheal intubation-induced epistaxis during various stages of anaesthesia ( at intubation , at extubation and during post op recovery upto 24 hours ).

Secondary

MeasureTime frame
Patient satisfaction following anesthesia procedure. Haemodynamic parameters during intervention Any other significant parameter. Timepoint: Patient satisfaction following anesthesia procedure. Haemodynamic parameters during intervention Any other significant parameter.

Countries

India

Contacts

Public ContactDinesh Kaushal

King Georges Medical University Lucknow

dineshkaushal91@yahoo.com9839089242

Outcome results

None listed

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