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Effect of intraoperative Ethanol injection to nerve ganglions on pain intensity after surgical resection of gastric and pancreatic masses

Pain relieving effect of intra-operative chemical splanchnicectomy of celiac ganglions in patients with resectable pancreatic or gastric masses: a randomized clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015022821269N1
Enrollment
44
Registered
2015-10-30
Start date
2015-04-21
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Condition 1: Pain intensity after gastric or pancreatic neoplasm resection. Condition 2: Resectable malignant neoplasm of head of pancreas. Condition 3: Resectable malignant neoplasm of stomach. Pain localized to upper abdomen Malignant neoplasm of head of pancreas Malignant neoplasm of stomach

Interventions

Intervention 1: no injection into control group during operation. Intervention 2: Injection of 20cc of prepared ethanol solution to each of celiac ganglions at both sides of supra-pancreatic portion o
Placebo
Treatment - Drugs
no injection into control group during operation
Injection of 20cc of prepared ethanol solution to each of celiac ganglions at both sides of supra-pancreatic portion of aorta.

Sponsors

Vice chancellor for research, Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Resectable pancreatic cancer or gastric cancer; Obtaining informed consent for probable alcohol injection during surgery. Exclusion criteria: Unresectable pancreatic cancer; Unresectable gastric cancer; Patients those who underwent neo-adjuvant chemotherapy; Patients who dissatisfaction with the procedures; Patients who expires before 4 month after operation; Prolonged post-operation hospitalization (more than 15 days) due to surgical complications; Age less than 15 or more than 80 year; History of prolonged consumption of opioids, NSAIDS, analgesic and anti-depressant drugs; Cardiac or pulmonary diseases; Sensitivity to opioid drugs; Psychological disorders; Abnormal arterial blood gas analysis; Happening of surgical complications or any other signs that results in disability to complete pain scale questionnaire (such as loss of consciousness).

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Severity of abdominal pain. Timepoint: Before surgery, one, two and four days after surgery, discharge time, one, two and four months after surgery. Method of measurement: Visual Analogue Scale (VAS) questionnaire.

Secondary

MeasureTime frame
Hospitalization time. Timepoint: Discharge time. Method of measurement: Number of days that patient stays at hospital after surgery.;Gastroparesia. Timepoint: Along first 72 hours after surgery. Method of measurement: Nausea, vomiting and volume of nasogastric tube secretions.;Arrhythmia or bradycardia. Timepoint: Along 72 hours after surgery. Method of measurement: Electrocardiography and cardiac monitoring.;Blood pressure. Timepoint: Every 30 minutes along 72 hours after operation. Method of measurement: Systolic and diastolic blood pressure will be measured by stethoscope and aneroid sphygmomanometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAmir Saraee

Firouzgar General Hospital

Dr.a.saraee@gmail.com; Saraee.a@tak.iums.ac.ir+98 21 2286 4438

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026