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Completed

NCT Number: NCT05966246

The Effect of Prucalopride Succinate on Gastrointestinal Motility After Laparoscopic Gastrectomy : Prospective Double Blind Case-control Study

In order to improve postoperative ileus in patients undergoing gastrointestinal surgery, digestive medications and prokinetics have been routinely used. Among them, mosapride citrate is widely used as a representative drug, as it is a 5-hydroxytryptamine 4 receptor agonist that increases gastrointestinal motility.

Prucalopride succinate (dihydrobenzofurancarboxamide) is a type of 5-hydroxytryptamine 4 receptor agonist that has a higher affinity for the 5-HT4 receptor compared to mosapride (a benzamide derivative) which belongs to the same class of drugs. Prucalopride succinate has been demonstrated to increase both gastric and colonic motility through in vivo and in vitro studies. As mentioned earlier, it exhibits high specificity for the 5-HT4 receptor. The 5-HT4 receptor is not expressed in the gastric mucosa but is expressed at low concentrations in the small intestine, whereas it is highly expressed in the colonic mucosa. Therefore, prucalopride is widely used as a therapeutic agent for chronic constipation by increasing colonic motility. Furthermore, Prucalopride succinate stimulates the 5-HT4 receptors present in the nerve terminals of the myenteric plexus, promoting the release of acetylcholine. The released acetylcholine acts on α7nAch receptors located on the surface of enteric smooth muscle cells, inhibiting inflammatory responses and reducing postoperative ilues.

A randomized controlled trial (RCT) conducted on 110 patients who underwent gastrointestinal surgery demonstrated that prucalopride succinate showed significant improvement in gastrointestinal motility compared to the control group. Currently, mosapride citrate is widely used as a prokinetic agent in clinical practice. However, preliminary studies have shown no significant efficacy, and when comparing abdominal X-ray images taken on the third day after surgery, there is no significant difference compared to the placebo group. As a result, it can be observed that the recovery of gastrointestinal motility after surgery is not primarily due to small bowel motility but rather delayed gas passing caused by colon motility. Therefore, it can be assumed that using drugs that increase colon motility may be effective in improving gastrointestinal motility after surgery.

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Key information

Age range

19 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

GangnamSeverance Hospital

Seoul, South Korea

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients diagnosed with gastric adenocarcinoma pathologically before surgery
  • Patients who underwent complete surgical resection (R0 resection)
  • Patients with an ASA score of 3 or less

Exclusion criteria

  • Patients over 80 years of age
  • Ascites or peritoneal metastasis
  • If you have intestinal obstruction before surgery
  • If chemotherapy was performed before surgery
  • If cancer other than gastric cancer is diagnosed
  • If there is a history of previous major intra-abdominal long-term surgery or abdominal radiation therapy
  • In case of liver failure or renal failure
  • Pregnant women
  • If it is judged that uncontrolled diabetes can affect intestinal function
  • If you have a stoma

Treatment and study plan

Arm I : Experimental (Prucalopride succinate group)

Drug

Experimental group taking prucalopride succinate from day 1 to day 5 after surgery

Arm II : Control (Mosapride citrate group)

Drug

Control gourp taking mosapride citrate from day 1 day 5 after surgery

Primary outcomes

  1. Quantitative intestinal motility measurement using radio-opaque markers

    Time frame: Every day from the 1st day to the 5th day after surgery

Secondary outcomes

  1. Measurement of the amount of food intake, first flatus time and first defecation time

    Time frame: Every day from the 1st day to the 5th day after surgery

    • Quantitatively compare and analyze the amount of food eaten in the test group and the control group.
    • Compare the first flatus appearance time and first defecation time in the test group and the control group.

Sponsors and collaborators

Lead sponsor

Gangnam Severance Hospital

Other

Registry information

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
Jul 28, 2023
Registry last updated
Aug 18, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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