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Efficacy of different analgesic regimens in the treatment of pain after arthroscopic shoulder surgery: a randomized controlled study

Efficacy of different analgesic regimens in the treatment of pain after arthroscopic shoulder surgery: a randomized controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200061181
Enrollment
Unknown
Registered
2022-06-15
Start date
2022-04-01
Completion date
Unknown
Last updated
2024-05-13

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

Conditions

Shoulder disease

Interventions

Experimental group 1:Dexamethasone 2 ml (10 mg) was injected intravenously, and ropivacaine 100 mg, dexmedetomidine 50 µg and magnesium sulfate 250 mg were given for supraclavicular brachial plexus bl
Experimental group 2:2 ml of normal saline was injected intravenously, and 100 mg of ropivacaine, 50 µg of dexmedetomidine and 250 mg of magnesium sulfate were given in the supraclavicular brachial pl
Experimental group 3:2 ml of normal saline was injected intravenously, and 100 mg of ropivacaine and 250 mg of magnesium sulfate were given in the supraclavicular brachial plexus block.
Experimental group 4:2 ml of normal saline was injected intravenously, and 100 mg of ropivacaine and 50 µg of dexmedetomidine were given in the supraclavicular brachial plexus block.

Sponsors

The Second Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Age between 18-65 years; 2. BMI 18-26; 3. ASA level 1-3; 4. Patients to undergo unilateral shoulder arthroscopy; 5. Agreed to accept the study and willing to complete the follow-up process.

Exclusion criteria

Exclusion criteria: 1. Allergic to related narcotic drugs; 2. Contraindications to brachial plexus block, such as coagulation dysfunction and local infection; 3. Patients with chronic pain and long-term use of analgesics before operation; 4. Patients with cognitive impairment who could not cooperate with postoperative pain assessment; 5. Pregnant and diabetes patients; 6. Liver and kidney dysfunction; 7. Reject participants.

Design outcomes

Primary

MeasureTime frame
Time of first request for analgesia;Cumulative opioid consumption;

Secondary

MeasureTime frame
Postoperative VAS score;Nausea and vomiting in patients within 24 hours after surgery;Patient satisfaction on the second postoperative day;Motor block duration;Duration of sensory block;Postoperative neurological complications (persistent numbness, paresthesia, and weakness);Shoulder joint American Shoulder and Elbow Surgeons Society score (ASES score) at discharge;Outcome length of stay;

Countries

China

Contacts

Public ContactMao Nie

The Second Affiliated Hospital of Chongqing Medical University

302218@cqmu.edu.cn+86 136 7842 8205

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 6, 2026