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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02323958
Other study ID # XJH-A-2014-6-26-01
Secondary ID
Status Completed
Phase N/A
First received December 8, 2014
Last updated July 25, 2017
Start date December 2014
Est. completion date December 2016

Study information

Verified date July 2017
Source Fourth Military Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is to observe whether transcutaneous electrical stimulation at specific acupoints could improve the quality of emergence in patients undergoing robotic laparoscopic gynecologic surgery.


Description:

During robotic laparoscopic gynecologic surgery, the patients are put in an extremely trendelenburg positon. And a long duration of this position could lead to delayed emergence or agitation. Stimulation at some acupoints were reported to improve homeostasis. In this study we tend to observe whether transcutaneous electrical stimulation at specific acupoints could improve the quality of emergence in patients undergoing robotic laparoscopic gynecologic surgery.


Recruitment information / eligibility

Status Completed
Enrollment 150
Est. completion date December 2016
Est. primary completion date September 2016
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Patients scheduled for robotic laparoscopic gynecologic surgery under general anesthesia

- Patients with written informed consent

Exclusion Criteria:

- Patients with difficulty in communication

- Patients with disease of central nervous system

Study Design


Related Conditions & MeSH terms


Intervention

Other:
acupoint stimulation
stimulation is given at acupoints
non-acupoint stimulation
stimulation is given at acupoints
electrode attached
electrodes are attached to skin
Device:
electrical stimulation
electrical stimulation is given through electrodes attached to th skin

Locations

Country Name City State
China Xijing Hospital Xi'an Shaanxi

Sponsors (1)

Lead Sponsor Collaborator
Fourth Military Medical University

Country where clinical trial is conducted

China, 

References & Publications (2)

Pandey R, Garg R, Darlong V, Punj J, Chandralekha, Kumar A. Unpredicted neurological complications after robotic laparoscopic radical cystectomy and ileal conduit formation in steep trendelenburg position: two case reports. Acta Anaesthesiol Belg. 2010;61 — View Citation

Schramm P, Treiber AH, Berres M, Pestel G, Engelhard K, Werner C, Closhen D. Time course of cerebrovascular autoregulation during extreme Trendelenburg position for robotic-assisted prostatic surgery. Anaesthesia. 2014 Jan;69(1):58-63. doi: 10.1111/anae.1 — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Time to awake time to open eyes to verbal command from end of inhaling sevoflurane to departing from postanesthesia care unit(PACU),an anticipated average of 1 hour
Secondary Richmond Score status of the patients during emergence from end of inhaling sevoflurane to departing from PACU,an anticipated average of 1 hour
Secondary Time to extubation from end of inhaling sevoflurane to departing from PACU,an anticipated average of 1 hour
Secondary QoR-15 Score of quality of recovery using a 15 items questionaire from end of inhaling sevoflurane to 24h after surgery,an anticipated average of 24 hour
Secondary residual sedation from arriving at PACU to departing from PACU,an anticipated average of 30min
Secondary PONV postoperative nausea and vomiting in the PACU from arriving at PACU to departing from PACU,an anticipated average of 30min
Secondary VAS score visual analogue score of pain in the PACU, scored 0-10 from arriving at PACU to departing from PACU,an anticipated average of 30min
Secondary serum Aquaporin 4 level of serum Aquaporin 4 before anesthesia and at the end of the surgery from before anesthesia to after surgery, an anticipated average of 4 hours
Secondary serum MMP9 level of serum Matrix metallop roteinase before anesthesia and at the end of the surgery from before anesthesia to after surgery, an anticipated average of 4 hours
Secondary serum S100ß level of serum S100ß before anesthesia and at the end of the surgery from before anesthesia to after surgery, an anticipated average of 4 hours
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