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Clinical observation for single intravenous preinjection of ketorolac tromethamine to inhibit cough caused by sufentanil during induction of general anesthesia

Clinical observation for single intravenous preinjection of ketorolac tromethamine to inhibit cough caused by sufentanil during induction of general anesthesia

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000030287
Enrollment
Unknown
Registered
2020-02-27
Start date
2020-02-29
Completion date
Unknown
Last updated
2020-03-02

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

Conditions

Cough caused by sufentanil during general anesthesia induction

Interventions

control group:Normal saline
experimental group:Intravenous injection of 0.5mg ketorolac tromethamine before anesthesia

Sponsors

Suqian People's Hospital of Nanjing Drum-Tower Hospital Group
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged 18~65 years old; 2. BMI: 18~30kg/m2; 3. ASA I~II grade; 4. Patients to be operataed on elective general anesthesia surgery.

Exclusion criteria

Exclusion criteria: 1. Pregnancy or lactation women; 2. With a history of drug allergy; 3. With cognitive or mental illness; 4. With severe cardiovascular and cerebrovascular diseases, liver, kidney and hematopoietic diseases; 5. Long-term use of analgesics or hormones, drug abuse History; 6. Those who participated in other clinical trials or researchers considered inappropriate to participate in this experiment.

Design outcomes

Primary

MeasureTime frame
Coughing times;

Secondary

MeasureTime frame
Mean arterial pressure;Heart rate;pulse oxygen saturation;Dosage of anesthetic drug;Side effects of anesthesia during resuscitation;

Countries

China

Contacts

Public ContactTian Zhen

Suqian People's Hospital of Nanjing Drum-Tower Hospital Group

tianzhen1000@126.com+86 15261204303

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 26, 2026