Appendicitis Clinical Trial
Official title:
Randomised Control Trial: Polymer Clips Versus Endoloops for Closure of the Appendiceal Stump During Emergency Laparoscopic Appendicectomy (The PECAS Trial)
The investigators propose a study to compare two methods of closing the stump of the
appendix during an emergency excision of the appendix using a keyhole approach. One
similarly designed study has been undertaken in another institution but there were not
enough patients recruited to the study to allow meaningful conclusions to be drawn.
Any patient over the age of 16 years whom the investigators suspect to have acute
appendicitis will be considered for recruitment to the study. During their exploratory
keyhole surgery, if the surgical team feels that excision of the appendix is indicated then
the patient will be randomly allocated to either polymer clips or endoloops to the part of
the procedure where the stump (base) of the appendix is closed.
The main aim is to determine if polymer clips shorten the duration of the operation. The
investigators will also determine if there is a difference between the rates of
complications, the time spent in hospital and the number of times the participants had to be
readmitted to hospital within 30 days.
The investigators propose to perform a randomised control trial within NHS Tayside comparing
two forms of appendiceal stump closure in emergency laparoscopic appendicectomy. A previous
RCT examining this topic could have been better designed, with a small trial population and
the absence of a power calculation.
All patients over 16 years old undergoing diagnostic laparoscopy for acute appendicitis will
be eligible for recruitment to the trial and be consented prior to theatre.
Intra-operatively, when the decision to perform an appendicectomy is taken, participants
will be randomised to either the application of polymer (Locaclip) clips or endoloops to the
appendiceal stump for closure during laparoscopic appendicectomy. The primary outcome will
be operative time, while secondary outcomes include post-operative complications length of
hospital stay and re-admission rate within 30 days. Participants will require no formal
follow-up, either in the out-patient clinic or telephone consultations.
Statistical analysis will predominantly use Fisher's exact test to determine any
statistically significant differences between each intervention arm, whilst group
homogeneity will be analysed for other important patient parameters.
The investigators hypothesise that the operative time will be less in the polymer group
compared to the endoloop group, while no significant difference will be seen in
post-operative complications or other secondary outcomes between the two cohorts. The
results of this RCT will add to the evidence-base for the use of polymer clips in
appendiceal stump closure and potentially support its use for routine clinical practice. It
is anticipated that it will take one year to recruit participants for the study and a
further 30 days to complete follow up for the last participant recruited.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment
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