Trial reportBMC surgery2026
Efficacy and safety of baclofen in the prophylaxis of postoperative nausea and vomiting after laparoscopic sleeve gastrectomy: a randomized controlled trial.
Trial report in BMC surgery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05516953 (Clinical Study Evaluating the Efficacy of Baclofen in Preventing Postoperative Nausea and Vomiting After Laparoscopic Sleeve Gastrectomy), which is not on this map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Clinical Study Evaluating the Efficacy of Baclofen in Preventing Postoperative Nausea and Vomiting After Laparoscopic Sleeve Gastrectomy
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundPostoperative nausea and vomiting (PONV) are among the most distressing aspects of the surgical experience, especially after laparoscopic sleeve gastrectomy (LSG). This study evaluated the efficacy and safety of baclofen for preventing PONV in patients with morbid obesity undergoing LSG.
methodsIn this double-blind placebo-controlled parallel study, 100 morbidly obese patients scheduled for LSG were randomized into two groups: the control group (n = 50), which received placebo and the baclofen group (n = 50), which received 10 mg of oral baclofen one hour before the anticipated time of surgery. The severity of PONV was assessed using the Rhodes index, and the frequency of rescue analgesia and pain intensity during the first 48 h after anaesthesia were evaluated using a visual analogue scale (VAS). Serum levels of substance P, serotonin, and vasopressin at baseline and 24 h after surgery were also evaluated.
resultsAs compared to the control group, baclofen treated group exhibited significant decline in the severity of PONV during the first 24 h postoperatively (P = 0.001), a significantly lower frequency of rescue analgesia doses needed during the first 24 h postoperatively (P = 0.001), a significantly lower pain intensity at 0–2 h, 6 h and 12 h postoperatively (P = 0.001) and significantly lower serum levels of substance P, serotonin, and vasopressin (P = 0.001). Moreover, baclofen was safe and tolerable, and its implication was not associated with excessive sedation or extrapyramidal side effects.
conclusionBaclofen could emerge as a promising new safe cost-effective agent for preventing PONV after LSG. CLINICAL
trial registrationClinicalTrials.gov Identifier: NCT05516953. Date of registration: 08/24/2022. URL: https://register.clinicaltrials.gov/prs/beta/studies/S000CF8D00000049/recordSummary .
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.