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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02523846
Other study ID # 20790
Secondary ID
Status Recruiting
Phase Phase 4
First received August 10, 2015
Last updated August 14, 2015
Start date August 2015

Study information

Verified date August 2015
Source Clinical Research Centre, Malaysia
Contact Lee Choo Yeoh, Master
Phone 047722625
Email yeohlc55@yahoo.com
Is FDA regulated No
Health authority Malaysia: Malaysia National Medical Research Registry
Study type Interventional

Clinical Trial Summary

The purpose of this study is to improve IV-Patient Controlled Analgesia (IV-PCA) technique for postoperative analgesia. Investigators are comparing between patient re-education and the background morphine infusion among patients who fail to achieve satisfactory analgesia using IV-PCA Morphine after laparotomy.


Description:

In this study, investigators have a second inclusion criteria for subject recruitment. For subjects who meet this criteria meaning their dynamic pain (when blowing incentive spirometer) is ≥ 4/10 after starting on IV-PCA Morphine will be randomized in to 2 groups. One group will receive patient re-‐education with an additional background morphine infusion and the other group will receive re-‐education only.

The second highlight for this study is regarding the background morphine calculation. The background morphine is calculated according to this formula:

Total morphine requirement in the first 24 hours post surgery (mg) = 100 - Age (year) So, the background morphine infusion will be calculated based on subject's age and half of their 24 hours requirement will be infused over 24 hours.

This formula was published by Pamela Macintyre in her paper titled " Age is the Best Predictor of Postoperative Morphine Requirement".


Recruitment information / eligibility

Status Recruiting
Enrollment 160
Est. completion date
Est. primary completion date July 2016
Accepts healthy volunteers No
Gender Both
Age group 20 Years to 70 Years
Eligibility Inclusion Criteria:

- American Society of Anesthesiologists (ASA)Physical Status Classification Class I and II

- Elective laparotomy

- able to understand either malaysia, mandarin, english language or local dialect

- patient with dynamic pain score 4/10 and more within the first 4-hour after initiation of IV-PCA

Exclusion Criteria:

- patient refusal

- laparotomy with pfannenstiel incision

- patients with a history of allergy to opioids

- patients who required post-operative ventilation support

- patients ASA III and above

- patients unable to use PCA due to insufficient comprehension

- morbid obesity/ obstructive sleep apnea

- chronic opioid or alcohol abuse

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
morphine
Investigators use the formula that was published by Pamela Macintyre in her paper entitled "Age is the Best Predictor of Postoperative Morphine Requirements." The estimation for the first 24-hour morphine requirement after surgery is calculated as: 100 - age (year). So, half of the total 24-hour morphine requirement will be infused over 24 hours. e.g. background morphine infusion= (100-Age)/ 2/ 24 (mg/hour)
Behavioral:
Patient re-education
A similar leaflet will be used to re-educate patient at 4 hour after surgery. The correct method to initiate IV-PCA dose, possible side effects and addiction issue will be explained again and re-emphasized

Locations

Country Name City State
Malaysia Sultanah Bahiyah Hospital Alor Seatr Kedah

Sponsors (1)

Lead Sponsor Collaborator
Clinical Research Centre, Malaysia

Country where clinical trial is conducted

Malaysia, 

References & Publications (1)

Macintyre PE, Jarvis DA. Age is the best predictor of postoperative morphine requirements. Pain. 1996 Feb;64(2):357-64. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary measure pain intensity at rest and when blowing incentive spirometer (dynamic pain) use combination of Numerical Rating Scale(NRS) and Visual Analogue Scale(VAS) 48 hours after surgery No
Secondary respiratory rate 48 hours after surgery Yes
Secondary total accumulative morphine consumption from IV-PCA pump 48 hours after surgery Yes
Secondary sedation level sedation score (0 to 3) 48 hours after surgery Yes
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