Trial · NCT07440758
Low-Flow Sevoflurane and Desflurane Anesthesia in Laparoscopic Cholecystectomy
NCT07440758, Not applicable, Completed, Kayseri City Hospital
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Low-Flow Sevoflurane and Desflurane Anesthesia in Laparoscopic Cholecystectomy. Trials, record NCT07440758. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07440758
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Low-Flow Sevoflurane and Desflurane Anesthesia in Laparoscopic Cholecystectomy
- NCT number
- NCT07440758
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 80 participants, actual
- Lead sponsor
- Kayseri City Hospital
- Conditions
- Laparoscopic Cholecystectomy, Postoperative Sore Throat
- Interventions
- Sevoflurane, Desflurane
- First posted
- 2026-02-27
- Last updated
- 2026-08-25
Source ClinicalTrials.gov
Registered outcomes8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Presence of Postoperative Sore Throat | 0, 2, 4, and 24 hours postoperatively | Presence (yes/no) at predefined postoperative time points. |
| Secondary | Severity of Postoperative Sore Throat | 0, 2, 4, and 24 hours postoperatively | Severity of postoperative sore throat assessed using a 4-point scale (0 = none, 1 = mild, 2 = moderate, 3 = severe) at predefined postoperative time points. |
| Secondary | Postoperative hoarseness | 0, 2, 4, and 24 hours postoperatively | Presence (yes/no) and severity of postoperative hoarseness assessed using a 4-point scale (0 = none, 1 = mild, 2 = moderate, 3 = severe). |
| Secondary | Postoperative Cough | 0, 2, 4, and 24 hours postoperatively | Presence and severity of postoperative cough assessed using a 4-point scale (0 = none, 1 = mild, 2 = moderate, 3 = severe). |
| Secondary | Postoperative Dysphagia (Difficulty Swallowing) | 0, 2, 4, and 24 hours postoperatively | Presence of foreign body sensation in the throat will be assessed as a dichotomous variable (Yes/No). |
| Secondary | Presence and Severity of Postoperative Nausea and Vomiting (PONV) | At postoperative 0, 2, 4, and 24 hours | Presence and severity of postoperative nausea and vomiting assessed using a standardized 4-point scale (0 = none, 1 = mild, 2 = moderate, 3 = severe). The need for rescue antiemetic medication. |
| Secondary | Intraoperative Consumption of Inhalational Anesthetic Agents | Intraoperative period | Total intraoperative consumption of inhalational anesthetic agents (sevoflurane or desflurane) measured during surgery. |
| Secondary | Patient Satisfaction (5-Point Likert Scale) | 24. hours postoperatively | Patient satisfaction will be assessed using a 5-point Likert scale consisting of the following response options: 1 = very dissatisfied, 2 = dissatisfied, 3 = neither satisfied nor dissatisfied, 4 = satisfied, and 5 = very satisfied. |
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/NCT07440758
GET https://conductscience.org/api/trials/v1/NCT07440758/registered