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Pharyngeal packs during surgery

Effect of pharyngeal packs during septorhinoplasty surgery on post operative sore throat and nausea and vomiting

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013011012094N1
Enrollment
90
Registered
2013-05-27
Start date
2013-03-10
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

septorhynoplasty. Deviated nasal septum

Interventions

Intervention 1: Intervention group A: after induction of anesthesia, a simple cotton gauze (16-layer) put in pharyngeal space by anesthesiologist. Intervention 2: Intervention group B: without pharyng
Prevention
Intervention group A: after induction of anesthesia, a simple cotton gauze (16-layer) put in pharyngeal space by anesthesiologist.
Intervention group B: without pharyngeal pack

Sponsors

Vice Chancellor for Research, Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: after regional ethical committee approval and written informed consent to participate in the study, all ASAI-II patients candid septorhinoplasty. Exclusion criteria: history of motion sickness; common cold with sore throat; consumption of analgesics in the past 48 hours; a history of substance abuse and smoking; difficult intubation and repeat laryngoscopy

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Nausea & Vomiting. Timepoint: Post operative times:0 (recovery), 2 , 6 and 24 h. Method of measurement: Nausea: No or Yes (mild or severe), vomiting: Yes or No.;Sore throat. Timepoint: Post operative times:0 (recovery), 2 , 6 and 24 h. Method of measurement: Visual analog scale(VAS): Pain from 0=no pain to 10=sever pain.

Secondary

MeasureTime frame
Duration of surgery. Timepoint: Beginning of anesthesia until extubation. Method of measurement: Hour.;Concomitant disease. Timepoint: Questionnaire preoperatively. Method of measurement: Patient history.;Receiving narcotic. Timepoint: Postoperative time. Method of measurement: The number of narcotic injection. Recorded in the questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Majid Razavi

Mashhad University of Medical Sciences

Razavim@mums.ac.ir; Majmrazavi@yahoo.com+98 51 1852 5209

Outcome results

None listed

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