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Effect of preoperative chewing-gum duration on postoperative sore throat and surgical-site pain in patients undergoing gynecological laparoscopic surgery under general anesthesia: a multicenter randomized controlled trial

Effect of preoperative chewing-gum duration on postoperative sore throat and surgical-site pain in patients undergoing gynecological laparoscopic surgery under general anesthesia: a multicenter randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500113121
Enrollment
Unknown
Registered
2025-11-25
Start date
2025-11-26
Completion date
Unknown
Last updated
2025-12-01

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

Conditions

postoperative sore throat and surgical-site pain

Interventions

Long term chewing gum group before surgery:Chew gum for 15 minutes before the operation
Short term chewing gum group before surgery:Chew gum for 2 minutes before the operation

Sponsors

Obstetrics and Gynecology Hospital of Fudan University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Age 20-65 years; (2) ASA physical status I or II; (3) Scheduled for elective gynecologic laparoscopic surgery under general anesthesia with endotracheal intubation, with an expected duration <=3 hours; (4) No history of chronic pain; (5) Capable of understanding the study, providing informed consent, and voluntarily participating in accordance with GCP guidelines.

Exclusion criteria

Exclusion criteria: (1) BMI >=30 kg/m^2; (2) Preexisting sore throat, hoarseness, dysphagia, or pharyngeal/ esophageal dysfunction; (3) History of oral or pharyngeal surgery; (4) History of chronic respiratory diseases; (5) History of gastroesophageal reflux disease; (6) Phenylketonuria (PKU); (7) Allergy to any medications used in this study; (8) Smoking within 7 days prior to surgery; (9) Use of NSAIDs within 14 days prior to surgery; (10) Use of corticosteroid therapy within 14 days prior to surgery; (11) History of opioid or alcohol abuse or dependence; (12) Unable to communicate normally; (13) Mallampati class >2; (14) Refusal to participate.

Design outcomes

Primary

MeasureTime frame
Incidence of moderate-to-severe postoperative sore throat within the first 24 hours;

Secondary

MeasureTime frame
NRS for postoperative sore throat;NRS for surgical-site pain;The incidence of bloodstains on the tip surface of the tracheal tube;The incidence of postoperative hoarseness;Preoperative anxiety score;Postoperative recovery quality score;

Countries

China

Contacts

Public ContactShaoqiang Huang

Obstetrics and Gynecology Hospital of Fudan University

timrobbins71@163.com+86 139 1821 0787

Outcome results

None listed

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