Pain, Postoperative Clinical Trial
— ShortstitchOfficial title:
Comparison Of Post-operative Pain In Short Versus Long Stitch Technique For Abdominal Wall Closure After Elective Laparotomy- A Double-Blind, Randomized Controlled Trial
| Verified date | January 2019 |
| Source | University of Malaya |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
Laparotomy is a surgical procedure where an incision is made through the abdominal wall in
order to gain access to the peritoneal cavity. Midline laparotomy incisions were the main
type of abdominal access. However, there were complications associated with laparotomy such
as incisional hernia, post-operative pain, surgical site infection and burst abdomen. The
anterior abdominal wall consists of skin, fascia, subcutaneous fat, external oblique
aponeurosis, internal oblique muscles, transversus abdominis and rectus muscles. The skin and
parietal peritoneum are supplied by T7- T12 and L1 nerve. Hence, breaching of the peritoneum,
giving rise to post-operative laparotomy pain. It is reported that approximately 60% of
patients who underwent laparotomy do complain of post-operative pain.
Techniques of abdominal wall closure has been constantly in order to develop an ideal suture
technique to minimise wound complications. One of the most significant changes in abdominal
closure technique was the introduction of mass closure technique, known as 'long stitch'
(LS). This conventional mass closure, uses a suture-to-wound length ratio (SL:WL) of 4:1,
achieved by the use of continuous sutures at one centimetre from rectus edge with
inter-suture distance of one centimetre. Studies have shown LS caused compression of tissues
enclosed in the mass stitch, leading to tissue ischaemia and necrosis. 'Short stitch' (SS)
was introduced in 1980s where it was reported to result in lower rate of incisional hernia
and surgical site infection. It has a SL:WL of more than four, achieved by placing the suture
five millimetres from rectus edge with inter-suture distance of five millimetre as well. It
incorporates only the linea alba, which may reduce tension and post-operative pain.Studies
has indicate that approximately 40% of post-operative patients reported inadequate pain
relief despite therapeutic intervention. Inadequate pain control is associated with
complications such as atelectasis, prolonged immobilization and hospital stay, thromboembolic
event, cardiac morbidity, insomnia, ileus and poor wound healing The Visual Analog Scale
(VAS) of pain is commonly used as measures of pain score or intensity in clinical trials. A
more objective way to evaluate the post-operative pain is to assess the usage of
patient-controlled analgesia (PCA) over a period of time. The commonly used PCA drug for
post-operative patient is morphine. As SS relies on less tension and proper distribution of
force along the fascial plane, it is possible that it might reduce post-operative pain as
compared to LS technique. It can be assessed using total usage of analgesia (intravenous
infusion or PCA), with correlation to the respective visual-analogue scales (VAS) or numeric
rating scales (NRS) at that particular time. There is no study that evaluate post-operative
pain difference between SS and LS technique.
The hypothesis of this study is that SS will reduce PCA morphine usage after midline
laparotomy, which translate into reduction in post-operative pain. In order to detect the 30%
reduction of PCA morphine, 86 patients are required.
| Status | Completed |
| Enrollment | 86 |
| Est. completion date | November 2018 |
| Est. primary completion date | November 2018 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: - Elective primary midline laparotomy, - ASA Class I to III - hemodynamically stable - able to provide consent for surgery Exclusion Criteria: - Emergency laparotomy - pregnancy - history of previous midline laparotomy - allergic to opiates - unable to use PCA morphine (handicapped) - patient will be planned for stoma creation |
| Country | Name | City | State |
|---|---|---|---|
| n/a | |||
| Lead Sponsor | Collaborator |
|---|---|
| University of Malaya |
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Reduction of PCA morphine usage post-operatively | Measure total usage of PCA morphine | 24 hours | |
| Secondary | Presence of Surgical site infection | Any surgical site infection at surgical site | throughout hospital stay, 2 weeks, 6 weeks and then 8 weeks during follow up (up to 1 year) | |
| Secondary | Length of hospital stay | number of days patient was admitted in the ward | since day 1 hospital admission until the time when patient is deemed fit to be discharged (up to 1 month) |
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