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Effect of Parecoxib on the Change of Shoulder Pain Threshold After Gynecological Laparoscopies

Primary Purpose

Postoperative Pain Management, Pain Threshold, Shoulder Pain, Laparoscopies

Status
Completed
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Parecoxib
Placebo
Sponsored by
First Affiliated Hospital, Sun Yat-Sen University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Postoperative Pain Management, Pain Threshold, Shoulder Pain, Laparoscopies focused on measuring NSAIDs, Hyperalgesia, Postlaparoscopic shoulder pain

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • females age 18-65yr,
  • American Society of Anesthesiologists (ASA)I-II,
  • Body Mass Index(BMI) 18-25kg/m2.

Exclusion Criteria:

  • a history of severe cardiac, pulmonary, hepatic, renal disease, chronic drug or alcohol abuse;
  • the presence of preoperative shoulder pain or any chronic pain syndrome, long-term use of analgesics; allergy or contraindications to nonsteroidal anti-inflammatory drugs (allergy, peptic ulcer disease, gastroesophageal reflux disease, renal insufficiency, coagulopathy) and any other drugs used in the study;
  • patient's pain evaluation is judged unreliable;
  • patients with conversion to a laparotomy;
  • refuse to coordinate with the follow-up tests.

Sites / Locations

  • Department of Anesthesiology, The First Affiliated Hospital, Sun Yat-sen University.

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Parecoxib

Placebo

Arm Description

Intravenously Parecoxib 40mg at 30min before intubation, 8h and 20h after surgery.

Normal saline 5ml will be intravenously infused at the same time points., respectively.

Outcomes

Primary Outcome Measures

The change of shoulder pressure pain threshold
The patients keep sitting position, and the pressure pain thresholds are measured twice at a fixed point in bilateral levator scapulae, supraspinatus, pectoralis major and flexor carpi ulnaris with a pressure algometer (FPX25, Wagner Instruments, USA) by an independent doctor.

Secondary Outcome Measures

The severity of shoulder pain
The patients are asked to rate the severity of shoulder pain via a visual analog scale (VAS) ranging from no pain (0) to worst possible pain (10) by another independent doctor.

Full Information

First Posted
April 23, 2013
Last Updated
February 15, 2014
Sponsor
First Affiliated Hospital, Sun Yat-Sen University
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1. Study Identification

Unique Protocol Identification Number
NCT01843010
Brief Title
Effect of Parecoxib on the Change of Shoulder Pain Threshold After Gynecological Laparoscopies
Official Title
Effect of Parecoxib on the Change of Shoulder Pain Threshold After Gynecological Laparoscopies
Study Type
Interventional

2. Study Status

Record Verification Date
February 2014
Overall Recruitment Status
Completed
Study Start Date
May 2013 (undefined)
Primary Completion Date
November 2013 (Actual)
Study Completion Date
November 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
First Affiliated Hospital, Sun Yat-Sen University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This prospective, double blind, placebo-controlled, parallel group study will be conducted in the first affiliated hospital of Sun yat-sen university in Guangzhou, China. Patients aged 18-65 (ASA I-II) undergoing elective gynecologic laparoscopic surgery with general anesthesia will be involved in this study. According to previous studies and our pilot trial, estimated 120 patients will be involved in this study. All eligible patients will be randomly assigned to two groups. In group P, patients will receive parecoxib 40mg intravenously 30min before intubation, 8h and 20h after the surgery,respectively. In Group C, patients will receive normal saline at the same time points. The shoulder pressure pain thresholds will be measured with a pressure algometer by an independent doctor blinding to medication and grouping at the day before surgery, 24h and 48h after surgery. Moreover, the intensity of shoulder pain and side effects will be evaluated by another independent doctor at 24h and 48h after surgery. At the end of the observation, the intensity of the maximal shoulder pain will be assessed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Postoperative Pain Management, Pain Threshold, Shoulder Pain, Laparoscopies
Keywords
NSAIDs, Hyperalgesia, Postlaparoscopic shoulder pain

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
140 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Parecoxib
Arm Type
Active Comparator
Arm Description
Intravenously Parecoxib 40mg at 30min before intubation, 8h and 20h after surgery.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Normal saline 5ml will be intravenously infused at the same time points., respectively.
Intervention Type
Drug
Intervention Name(s)
Parecoxib
Intervention Description
Parecoxib 40mg will be intravenously infused.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Normal saline 5ml will be intravenously infused.
Primary Outcome Measure Information:
Title
The change of shoulder pressure pain threshold
Description
The patients keep sitting position, and the pressure pain thresholds are measured twice at a fixed point in bilateral levator scapulae, supraspinatus, pectoralis major and flexor carpi ulnaris with a pressure algometer (FPX25, Wagner Instruments, USA) by an independent doctor.
Time Frame
The pressure pain thresholds are measured at the day before surgery, 24h and 48h after surgery
Secondary Outcome Measure Information:
Title
The severity of shoulder pain
Description
The patients are asked to rate the severity of shoulder pain via a visual analog scale (VAS) ranging from no pain (0) to worst possible pain (10) by another independent doctor.
Time Frame
At the day before surgery, 24h and 48h after surgery

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: females age 18-65yr, American Society of Anesthesiologists (ASA)I-II, Body Mass Index(BMI) 18-25kg/m2. Exclusion Criteria: a history of severe cardiac, pulmonary, hepatic, renal disease, chronic drug or alcohol abuse; the presence of preoperative shoulder pain or any chronic pain syndrome, long-term use of analgesics; allergy or contraindications to nonsteroidal anti-inflammatory drugs (allergy, peptic ulcer disease, gastroesophageal reflux disease, renal insufficiency, coagulopathy) and any other drugs used in the study; patient's pain evaluation is judged unreliable; patients with conversion to a laparotomy; refuse to coordinate with the follow-up tests.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ke xuan Liu, M.D and Ph.D
Organizational Affiliation
1st affiliated hospital of Sun Yat-sen university
Official's Role
Study Director
Facility Information:
Facility Name
Department of Anesthesiology, The First Affiliated Hospital, Sun Yat-sen University.
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510089
Country
China

12. IPD Sharing Statement

Citations:
PubMed Identifier
23136538
Citation
Zhang H, Shu H, Yang L, Cao M, Zhang J, Liu K, Xiao L, Zhang X. Multiple-, but not single-, dose of parecoxib reduces shoulder pain after gynecologic laparoscopy. Int J Med Sci. 2012;9(9):757-65. doi: 10.7150/ijms.4916. Epub 2012 Oct 23.
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Effect of Parecoxib on the Change of Shoulder Pain Threshold After Gynecological Laparoscopies

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