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Paragastric Neural Blockade and Laparoscopic Assisted Transversus Abdominis Plane Block on Visceral Pain After Surgery

ConditionVisceral Pain
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age20-50
SponsorAlexandria University

About this trial

after laparoscopic bariatric surgery, visceral pain (VP) remains a significant issue. VP causes autonomic symptoms, such as nausea and vomiting, and does not respond to conventional pain management methods that target incisional pain. The present study was performed to test the effect of use of combined paragastric autonomic neural blockade and laparoscopic assisted transversus abdominis plane block on visceral pain during laparoscopic bariatric surgery and in the early postoperative period.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age: 20-50 years, both sexes.

ASA physical status class I to III.

BMI 35- 50 kg/m²

Disqualifiers

Severe cardiac disorder

chronic renal failure

liver cirrhosis

allergy to bupivacaine

Trial design

Design model

Parallel

Treatments tested in this trial

  • combined paragastric autonomic neural blockade and laparoscopic assisted transversus abdominis plane block

    Procedure/Surgery

    paragastric autonomic neural blockade and laparoscopic assisted transversus abdominis plane block

  • laparoscopic assisted transversus abdominis plane block

    Procedure/Surgery

    laparoscopic assisted transversus abdominis plane block

Treatment groups

120 Participants
are divided into 2 treatment groups
Group A: Paragastric and transversus abdominis plane blockExperimental treatment 1 intervention
Group B: Transversus abdominis plane blockOther 1 intervention

Trial outcomes

Primary outcomes

1

postoperative pain score

VAS score

Time frame
postoperative day 1

Secondary outcomes

1

Number of patients who need opioids in postoperative period

number

Time frame
postoperative day 1
2

time to first dose of rescue analgesia

minutes

Time frame
postoperative day1
3

Postoperative nausea and vomiting

number

Time frame
postoperative day 1

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Alexandria University

Lead sponsor

Source ClinicalTrials.gov
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