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Clinical Trials/NCT01845532
NCT01845532CompletedNot Applicable

Analgesic Effect of Trigger Point Injection and EMLA for Shoulder Pain in Laparoscopic Hysterectomy

Yonsei University1 site in 1 country75 target enrollmentStarted: April 2013Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
75
Locations
1
Primary Endpoint
postoperative shoulder pain

Study Overview

Brief Summary

Laparoscopic operative procedures have revolutionized gynecological surgery. These have several advantages: a smaller and more cosmetic incision, reduced blood loss and shorter postoperative stay, which cuts down on hospital costs. However, postoperative pain continues to be one complication, which results in an unpleasant experience for the patient and at times causes a delayed discharge. Trigger point injection removes the pain developing point and block the pain signal. EMLA cream shows analgesic effect when being spread on the skin. An literature showed that patch of local anesthetics showed the effect of trigger point inject. The purpose of this study is to investigate the alleviation of shoulder pain, headache, abdominal pain, and back pain after trigger point injection or EMLA cream applying on shoulder in patients undergoing total laparoscopic hysterectomy.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
20 Years to 70 Years (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • ASA class I or II
  • age 20~70
  • patients undergoing total laparoscopic hysterectomy

Exclusion Criteria

  • history of shoulder surgery
  • coagulopathy
  • infection or trauma of shoulder
  • general inflammation
  • allergy to local anesthetics

Arms & Interventions

TPI group

Experimental

Intervention: TPI (Drug)

ELMA group

Active Comparator

Intervention: EMLA cream (Drug)

Outcomes

Primary Outcomes

postoperative shoulder pain

Time Frame: 3 hr after end of surgery

Postoperative shoulder pain is measured using the VAS at 3 hr after end of surgery.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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