Trial · NCT04485117
Propofol Versus Sevoflurane Anesthesia in Pediatric Strabismus Surgery: Feasibility of BIS Monitoring
NCT04485117, Not applicable, Completed, Sameh Fathy
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Propofol Versus Sevoflurane Anesthesia in Pediatric Strabismus Surgery: Feasibility of BIS Monitoring. Trials, record NCT04485117. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04485117
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Propofol Versus Sevoflurane Anesthesia in Pediatric Strabismus Surgery: Feasibility of BIS Monitoring
- NCT number
- NCT04485117
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 100 participants, actual
- Lead sponsor
- Sameh Fathy
- Conditions
- Strabismus
- Interventions
- Bispectral Index Monitor, Laryngeal Mask Airway, Sevoflurane, Propofol
- First posted
- 2020-07-24
- Last updated
- 2021-06-10
Source ClinicalTrials.gov
Registered outcomes9
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Incidence of oculocardiac reflex | Up to the end of the surgery | Any dysrhythmia or rapid reduction in HR by more than 25% from the baseline is taken as oculocardiac reflex. |
| Secondary | Changes in bispectral index | Up to the end of the surgery | Bispectral index values (0-100) are recorded every five minutes until the end of the surgery |
| Secondary | Changes in heart rate | Up to the end of the surgery | Heart rate (beat/min) is recorded at five-minute intervals until the end of the surgery |
| Secondary | Changes in mean arterial blood pressure | Up to the end of the surgery | Mean blood pressure (mmHg) is recorded at five-minute intervals until the end of the surgery |
| Secondary | Changes in postoperative emergence agitation scale | Up to 30 minutes after surgery | Agitation is assessed using the 5- step Cravero scale (1-5) every five minutes from awakening and for 30 minutes.(1:Obtunded with no response to stimulation, 2:Asleep but responsive to movement or stimulation, 3:Awake and responsive, 4:Crying, 5:Thrashing behaviour that requires restraint) |
| Secondary | Changes in postoperative pain score | Up to 24 hours after surgery | Pain score from 0 to 10 (0 = no pain and 10 = the worst imaginable pain) is assessed every two hours for 24 hours after surgery. |
| Secondary | First analgesic request | Up to 24 hours after surgery | The time of the first analgesic request for paracetamol is recorded. |
| Secondary | Total analgesic requirements of paracetamol | Up to 24 hours after surgery | The amount of paracetamol consumption given as a rescue analgesia to patients is measured all over the 24 hours. |
| Secondary | Incidence of postoperative nausea and vomiting | Up to 24 hours after surgery | Incidence of postoperative nausea and vomiting is assessed during the first 24 hours post-operatively. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT04485117
GET https://conductscience.org/api/trials/v1/NCT04485117/registered