Status:
COMPLETED
Superficial Cervical Plexus Block for Postoperative Analgesia
Lead Sponsor:
Beijing Tiantan Hospital
Conditions:
Plexus Block;Analgesia;Neurosurgery
Eligibility:
All Genders
18-65 years
Phase:
NA
Brief Summary
The incidence of postoperative pain after craniotomy is high. Severe postoperative pain can lead to a series of complications that are detrimental to the recovery of craniotomy patients. Compound loca...
Eligibility Criteria
Inclusion
- Elective suboccipital retrosigmoid approach approach craniotomy;
- Age between 18 and 65 years;
- American Society of Anesthesiologists (ASA) physical status I-III.
Exclusion
- The patients or legal clients refuse to provide informed consent;
- Local infection;
- Preoperative impairment of consciousness and cognitive function;
- Uncontrolled hypertension;
- Inability to communicate;
- Allergies to experimental drugs;
- History of drug abuse;
- History of chronic headache;
- Aphasia and hearing impairment;
- Patients undergoing second craniotomy;
- Body mass index \< 18.5 kg/m2 or \> 35.0 kg/m2;
Key Trial Info
Start Date :
November 18 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 10 2021
Estimated Enrollment :
106 Patients enrolled
Trial Details
Trial ID
NCT04036812
Start Date
November 18 2019
End Date
April 10 2021
Last Update
February 13 2025
Active Locations (2)
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1
Beijing Tiantan Hospital
Beijing, Beijing Municipality, China, 100050
2
Beijing TianTan Hospital
Beijing, China, 100070