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Efficacy of dexmedetomidine on postoperative pain in patients undergoing gastric and esophageal endoscopic submucosal dissection

Efficacy of dexmedetomidine on postoperative pain in patients undergoing gastric and esophageal endoscopic submucosal dissection

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100043837
Enrollment
Unknown
Registered
2022-03-04
Start date
2021-03-22
Completion date
Unknown
Last updated
2022-10-04

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

Conditions

gastric and esophygeal tumors

Interventions

Dex group:During the induction period of general anesthesia, dexmedetomidine with a concentration of 4 µ g / ml was administered intravenously at the rate of 1 µ g / kg for more than 10 minutes, follo
C ?:The same volume of saline with D group is administered during general anesthesia.

Sponsors

Beijing Friendship Hospital Affiliated to Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients aged 18-65 years, ASAI ~ II, scheduled for ESD surgery for gastric and esophageal tumors.

Exclusion criteria

Exclusion criteria: (1) Sinus bradycardia; (2) sick sinus syndrome; (3) predictable difficult airway or obesity (BMI > 35kg / cm2); (4) mental illness; (5) allergic to dexmedetomidine; (6) long-term history of opioid use; (7) refused follow-up or drug intervention after surgery.

Design outcomes

Primary

MeasureTime frame
visual analogue scales;

Secondary

MeasureTime frame
sedation score;postoperative nausea and vomiting(PONV) score;shivering score;satisfaction scores of patient at 48h;advert events;treatment and agents of posteoperative pain and rescue of adverse events;

Countries

China

Contacts

Public ContactLixin An

Beijing Friendship Hospital affiliated to Capital Medical University

anlixin8120@163.com+86 010-63138761

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 17, 2026