Nursing-Led ERAS Protocol for Improving Recovery After Emergency Laparotomy
NCT07920458, Not applicable, Completed, Al-Zaytoonah University of Jordan
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Nursing-Led ERAS Protocol for Improving Recovery After Emergency Laparotomy | ClinicalTrials.gov |
| NCT number | NCT07920458 | ClinicalTrials.gov |
| Status | Completed | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 120 participants, actual | ClinicalTrials.gov |
| Lead sponsor | Al-Zaytoonah University of Jordan | ClinicalTrials.gov |
| Conditions | Enhanced Recovery After Surgery (ERAS) Protocol | ClinicalTrials.gov |
| Interventions | Nursing-Led Enhanced Recovery After Surgery (ERAS) Protocol, Routine Postoperative Care | ClinicalTrials.gov |
| First posted | 2026-11-05 | ClinicalTrials.gov |
| Last updated | 2026-11-05 | ClinicalTrials.gov |
Registered outcomes 4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Postoperative Pain Intensity | Postoperative Days 1, 2, and 3. | Postoperative pain intensity was assessed using the Numeric Pain Rating Scale (NPRS), an 11-point scale ranging from 0 (no pain) to 10 (worst possible pain). Mean pain scores were compared between the study and control groups. | ClinicalTrials.gov |
| Primary | Time to First Passage of Flatus | From the end of surgery until the first documented passage of flatus or hospital discharge, whichever occurs first, during the postoperative hospitalization. | The time interval, measured in hours, from the end of emergency laparotomy surgery to the first documented passage of intestinal flatus. The time will be recorded from nursing documentation and compared between the study and control groups. | ClinicalTrials.gov |
| Primary | Time to First Bowel Movement | From the end of surgery until the first documented bowel movement or hospital discharge, whichever occurs first, during the postoperative hospitalization. | The time interval, measured in hours, from the end of emergency laparotomy surgery to the first documented bowel movement. The time will be recorded from nursing documentation and compared between the study and control groups. | ClinicalTrials.gov |
| Primary | Length of Hospital Stay | From the date of hospital admission until the date of hospital discharge during the index hospitalization. | Total duration of hospitalization, measured in days from hospital admission until hospital discharge. The duration will be calculated from admission and discharge dates documented in the patient's medical record and compared between the study and control groups. | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 0
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|
Grants 0
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.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years | Source |
|---|
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|
Source 5
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.4.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
| NIH clinical studies file | 2026-11-13 | ClinicalTrials.gov |
Release trials-2026-11-12-0.4.0
ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)