Evidence map›Paper›PMID 41152767›Full record

ArticleBMC anesthesiology2025

Comparison of the anesthetic efficacy and recovery quality of remimazolam besylate versus sevoflurane for pediatric circumcision: a single-center, prospective, assessor-blinded, randomized controlled study protocol.

Yi Zhang, Shuang Guo, Linyun Wang, Qingjun Zeng, Haishan Cui, Yunbo Mo

Abstract readClinical Trial Protocol
In one paragraph

Article in BMC anesthesiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Trial
  2. Trial
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Yi Zhang *Department of Anesthesiology, Maternal and Child Health Hospital of Wanzhou District, Chongqing City, People's Republic of China.ORCID http://orcid.org/0009-0009-1853-9358
Shuang Guo *Department of Anesthesiology, Maternal and Child Health Hospital of Wanzhou District, Chongqing City, People's Republic of China.ORCID http://orcid.org/0009-0009-2779-6444
Linyun WangNursing Department, Maternal and Child Health Hospital of Wanzhou District, Chongqing City, People's Republic of China.
Qingjun ZengDepartment of Anesthesiology, Maternal and Child Health Hospital of Wanzhou District, Chongqing City, People's Republic of China.
Haishan CuiDepartment of Anesthesiology, Maternal and Child Health Hospital of Wanzhou District, Chongqing City, People's Republic of China.
Yunbo MoDepartment of Pediatrics, Maternal and Child Health Hospital of Wanzhou District, Chongqing City, People's Republic of China. moyunbo666@outlook.com.

Funding

The Joint General Fund for Science, Health Science, and Technology in Wanzhou District, Chongqing, People's Republic of China wzwjw-kw2024031
6 · The paper itself

Abstract

backgroundAdministering anesthesia for circumcision in children involves prioritizing safety, comfort, and quality of recovery. While the effectiveness of remimazolam besylate in pediatric anesthesia requires additional confirmation, sevoflurane has been linked to complications like agitation and delirium upon recovery. This protocol describes a planned assessor-blinded randomized controlled trial to evaluate the anesthetic impacts, recovery features, and safety profiles of remimazolam compared to sevoflurane in children between the ages of 3 and 12 undergoing circumcision.

methodsThis single-center, prospective, assessor-blinded, randomized controlled trial will be conducted at the Wanzhou District Maternal and Child Health Hospital. One hundred children (aged 3-12 years, ASA I-II) scheduled for painless circumcision will be randomly allocated to receive either intravenous remimazolam besylate (Group R, n = 50) or inhaled sevoflurane (Group S, n = 50) for general anesthesia. Both groups will receive a penile root block with 1% lidocaine. Primary outcomes include time to achieve general anesthesia (MOAA/S ≤ 1) and emergence time. Secondary outcomes include anesthesia success rate, intraoperative interventions, hemodynamic changes, respiratory complications, emergence delirium (PAED scale), pain scores (FLACC), and guardian anxiety levels. Due to inherent differences in drug delivery methods, only outcome assessors and data analysts will be blinded. Exploratory subgroup analyses by age (3-6 vs. 7-12 years) will be conducted but are not powered for definitive conclusions. Statistical analysis will use SPSS version 26.0 with significance at P < 0.05. ETHICS AND DISSEMINATION: The Reproductive Ethics Committee at the Wanzhou District Maternal and Child Health Hospital has approved this protocol (Reference No. 2024-44). Consent from the legal guardians will be secured. Findings will be shared via publications in journals and presentations at academic conferences.

trial registrationThis trial has been registered with the Chinese Clinical Trial Registry (ChiCTR) (Registration number: ChiCTR2500095974; Registration date: January 15, 2025).

Indexed as

Anesthesia Recovery PeriodAnesthetics, InhalationBenzodiazepinesCircumcision, MaleSevofluraneAnesthesia, GeneralChildChild, PreschoolHumansMaleProspective StudiesRandomized Controlled Trials as TopicSingle-Blind MethodAnesthetics, InhalationBenzodiazepinesremimazolamSevofluraneAnesthetic effectAssessor-Blinded trialCircumcisionPediatric anesthesiaRecovery qualityRemimazolam besylateSevofluraneStratified randomizationStudy protocol

Identifiers

PMID41152767
PMCPMC12570819

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.