Trial · NCT07885358
Anesthesia Management and Perioperative Outcomes in Awake Jejunostomy and Gastrostomy
NCT07885358, Completed, Samsun University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Anesthesia Management and Perioperative Outcomes in Awake Jejunostomy and Gastrostomy. Trials, record NCT07885358. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07885358
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Anesthesia Management and Perioperative Outcomes in Awake Jejunostomy and Gastrostomy
- NCT number
- NCT07885358
- Status
- Completed
- Enrollment
- 16 participants, actual
- Lead sponsor
- Samsun University
- Conditions
- Jejunostomy, Gastrostomy, Anesthesia, Regional
- First posted
- 2026-10-21
- Last updated
- 2026-10-21
Source ClinicalTrials.gov
Registered outcomes9
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Completion of Surgery Without Conversion to General Anesthesia | "Perioperative/Periprocedural" | The proportion of patients in whom the planned surgical jejunostomy or gastrostomy was completed using a fascial plane block-based anesthetic strategy, with supplementary sedation or analgesia as clinically indicated, without conversion to general anesthesia. Conversion status was determined from the anesthesia records. The outcome was expressed as the number and percentage of patients, with an exact binomial 95% confidence interval. |
| Secondary | Supplementary Sedative and Analgesic Requirements | "Perioperative/Periprocedural" | The number and percentage of patients receiving supplementary intravenous sedative or analgesic medications during surgery, including midazolam, ketamine, propofol, and fentanyl, as documented in anesthesia records. |
| Secondary | New Airway Intervention | "Perioperative/Periprocedural" | The number and percentage of patients requiring a new airway intervention during surgery. Continuation of pre-existing mechanical ventilation through a tracheostomy was not classified as a new airway intervention. |
| Secondary | Intraoperative Adverse Events | "Perioperative/Periprocedural" | The number and percentage of patients with documented intraoperative hypotension, bradycardia, or oxygen desaturation, based on retrospective anesthesia records. Standardized numerical thresholds were not established in the available study description. |
| Secondary | Intraoperative Vasopressor Requirement | "Perioperative/Periprocedural" | The number and percentage of patients receiving vasopressor medication during the surgical procedure, as documented in anesthesia records. |
| Secondary | Postoperative Rescue Analgesic Requirement | postoperative 24 hours | The number and percentage of patients with documented administration of additional postoperative analgesics beyond routine intravenous paracetamol. |
| Secondary | Documented Early Postoperative Complications | postoperative 24 hours | The number and percentage of patients with early block-related or procedure-related complications documented in the reviewed hospital records. |
| Secondary | Postoperative Length of Hospital Stay | up to two months | The number of days from the surgical procedure to hospital discharge among patients discharged alive, summarized using the median and interquartile range. |
| Secondary | In-Hospital Mortality | up to two months | The number and percentage of patients who died during the index hospitalization following surgical jejunostomy or gastrostomy. Deaths documented within 30 days of surgery were also described. Complete 30-day all-cause mortality was not assessed. |
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/NCT07885358
GET https://conductscience.org/api/trials/v1/NCT07885358/registered