Clinical Trials Directory

Trials / Completed

CompletedNCT03648034

Effects of Scalp Nerve Block With Ropivacaine on Postoperative Recovery Quality

Effects of Preoperative Scalp Nerve Block on Postoperative Recovery Quality in Patients Undergoing Excision of Intracranial Meningioma

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
144 (actual)
Sponsor
RenJi Hospital · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

Patients undergoing elective meningeoma resection surgery will be randomly assigned to one of the following two groups. After anesthesia induction but before skull-pin insertion, one group will receive scalp nerve blocks with 0.5% ropivacaine, whereas the other group will receive scalp nerve blocks with 0.9% saline. The patients' postoperative recovery quality, which is evaluated by KPS score, peri-operative inflammatory responses, and post-operative pain degree will be evaluated and compared between the two groups.

Detailed description

Patients undergoing elective meningeoma resection surgery will be randomly assigned to one of the following two groups. After anesthesia induction but before skull-pin insertion, one group will receive scalp nerve blocks with 0.5% ropivacaine, whereas the other group will receive scalp nerve blocks with 0.9% saline. The patients' KPS scores at 3d after surgery and at discharge, serum levels of TNF-α、IL-6,IL-1β at 24h after surgery, satisfaction score after recovery, and VAS scores at 1, 2, 3 days post-surgery will be evaluated and compared between the two groups.

Conditions

Interventions

TypeNameDescription
PROCEDUREropivacaineTo perform scalp nerve blocks with ropivacaine
PROCEDUREsalineTo perform scalp nerve blocks with saline

Timeline

Start date
2018-09-18
Primary completion
2019-09-30
Completion
2019-11-30
First posted
2018-08-27
Last updated
2020-04-06

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT03648034. Inclusion in this directory is not an endorsement.