Implementation of a Pain Management Plan in Major Open Abdominal Surgeries.

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Record identity and dates

Source

ClinicalTrials.gov

Source record ID

NCT07901582

Title field or adapter rule

{'original_value': 'Implementation of a Pain Management Plan in Major Open Abdominal Surgeries.', 'source_field': 'protocolSection.identificationModule.officialTitle'}

Ingested At

2026-10-31T23:27:21.134537+00:00

Published At

2026-10-30T00:00:00+00:00

Record Updated At

2026-10-30

Source Retrieved At

2026-10-31T22:17:25.750886+00:00

Timestamp Basis

ClinicalTrials.gov API/RSS response retrieval timestamp recorded by Dossier adapter

Date limitation

ClinicalTrials.gov API/RSS response retrieval timestamp recorded by Dossier adapter

Fields recorded by this source

protocolSection.conditionsModule.conditions

["Abdomen Cancer", "Pancreas Adenocarcinoma (MSI-H)", "Colectomy Left/Right/Total Under Laparotomy", "Hepatectomy", "Nephrectomy", "Esophagectomy", "Pelvic Cancer, Enteritis, Probiotics,Chemoradiotherapy", "Hysterectomy and Salpingectomy and Oophorectomy", "Salpingectomy", "Open Abdominal Surgeries", "Adrenal Carcinoma", "Prostatectomy"]

protocolSection.statusModule.lastUpdatePostDateStruct

{"date": "2026-10-30", "type": "ACTUAL"}

protocolSection.identificationModule.nctId

"NCT07901582"

protocolSection.identificationModule.officialTitle

"Implementation of a Pain Management Plan in Major Open Abdominal Surgeries."

protocolSection.statusModule.overallStatus

"RECRUITING"

protocolSection.designModule.phases

["NA"]

protocolSection.statusModule.resultsFirstPostDateStruct

null

Study condition terms

• Abdomen Cancer (protocolSection.conditionsModule.conditions)
• Pancreas Adenocarcinoma (MSI-H) (protocolSection.conditionsModule.conditions)
• Colectomy Left/Right/Total Under Laparotomy (protocolSection.conditionsModule.conditions)
• Hepatectomy (protocolSection.conditionsModule.conditions)
• Nephrectomy (protocolSection.conditionsModule.conditions)
• Esophagectomy (protocolSection.conditionsModule.conditions)
• Pelvic Cancer, Enteritis, Probiotics,Chemoradiotherapy (protocolSection.conditionsModule.conditions)
• Hysterectomy and Salpingectomy and Oophorectomy (protocolSection.conditionsModule.conditions)
• Salpingectomy (protocolSection.conditionsModule.conditions)
• Open Abdominal Surgeries (protocolSection.conditionsModule.conditions)
• Adrenal Carcinoma (protocolSection.conditionsModule.conditions)
• Prostatectomy (protocolSection.conditionsModule.conditions)

Interventions recorded in this study

• {'armGroupLabels': ['Analgesic Combination-Fentanyl&Ropivacaine 0.2%'], 'description': 'Postoperative analgesic combination - Ropivacaine 200 ml/400 mg + Fentanyl for continuous epidural infusion for the first 5 days.The infusion will start 2 hours before the end of the operation and before the admission to the intensive care unit.', 'name': 'Epidural administered opioid', 'type': 'PROCEDURE'} (protocolSection.armsInterventionsModule.interventions[])
• {'armGroupLabels': ['Analgesic Combination-Morphine&Ropivacaine 0.2%'], 'description': 'Postoperative analgesic combination - Ropivacaine 200 ml/400 mg + Morphine for continuous epidural infusion for the first 5 days.The infusion will start 2 hours before the end of the operation and before the admission to the intensive care unit.', 'name': 'Epidural administered opioid', 'type': 'PROCEDURE'} (protocolSection.armsInterventionsModule.interventions[])

An intervention appearing in a study record does not establish an effect or an approved use.

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