ERCP: Complications After Endoscopic Retrograde Cholangiopancreatography

Sponsor
Juan Carlos Martín del Olmo (Other)
Overall Status
Completed
CT.gov ID
NCT04735224
Collaborator
(none)
500
47.6

Study Details

Study Description

Brief Summary

Retrospective study to analyze benign complications and malignancy risks after ERCP with sphincterotomy. All patients who received a ERCP with sphincterotomy for a benign disease will be included. Post-ERCP hepato-biliary complications in the follow-up will be registered.

Detailed Description

This is a single center retrospective study. All patients that received an ERCP with sphincterotomy for a benign disease from 1995 will be included.

The exclusion criteria are diagnosis of primary malignant tumors in the liver, bile ducts including peri-ampullary region and pancreas in the ERCP. Loss of follow-up less than two years after the ERCP and biliopancreatic malignancy diagnostic in this period. The initial work-up included laboratory test, ultrasound scan and, when precise, computed tomography (CT) and magnetic resonance image (MRI).

The data collected will be:
  1. Age, sex, comorbidities, long of hospital stay.

  2. ERCP indications.

  3. ERCP sphincterotomy or precut, biliary stent insertion and type of stent.

  4. post-ERCP diagnosis, abnormal diameter of biliary tree.

  5. ERCP repetition and causes.

  6. Immediate complications like bleeding, residual choledocholithiasis, ascending cholangitis, pancreatitis, and cholecystitis, and their number after more than two months.

  7. Malignant complications after more than two years: cholangiocarcinoma, hepatocarcinoma and ductal pancreatic adenocarcinoma.

Stistical analyses will be performed using SPSS, ver. 25.0 (SPSS Inc., Chicago Illinois, USA). The demographics, perioperative data, operation details, length of hospital stay, morbidity, mortality and pathologic and oncological outcomes are expressed as numbers and percentages for qualitative variables and medians and interquartile ranges (IQRs) for quantitative variables.

Univariate and multivariate logistic regression analyses will be employed to determine the risk factors for the development short-term and long-term complications. Variables with P<0.1 in the univariate analysis will be further introduced into the multivariate analysis with the Wald selection method. P values < 0.05 were considered statistically significant.

This study involved the use of data from clinical records. To guarantee the proper handling of the information, the data were treated confidentially and anonymously according to the provisions of the Spanish Organic Law 15/1999, of 13 December 1999, on Personal Data Protection (LOPD). All methods were performed in accordance with the guidelines and regulations established by the Declaration of Helsinki (1964, revised in 1983) on biomedical research in humans, the Spanish Royal Decree 1090/2015, of December 4, which regulates clinical trials with drugs, the Research Ethics Committees with drugs and the Spanish Registry of Clinical Studies. Ethical approval from the Clinical Trials and Ethics Committee of Valladolid University was granted.

Study Design

Study Type:
Observational
Actual Enrollment :
500 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Long-term Risks After Endoscopic Retrograde Cholangiopancreatography (ERCP) With Sphincterotomy.
Actual Study Start Date :
Jan 1, 2017
Actual Primary Completion Date :
Oct 10, 2020
Actual Study Completion Date :
Dec 20, 2020

Outcome Measures

Primary Outcome Measures

  1. long-term complications after ERCP with sphincterotomy [10 years]

    Long- terms complications registered

Secondary Outcome Measures

  1. characteristics of patients who develop complications after endoscopy sphincterotomy [10 years]

    defined characteristics

Other Outcome Measures

  1. association between ERCP with sphincterotomy and the development of neoplasm in the bile ducts [10 years]

    risks of malignancy

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Inclusion Criteria:
  • Patients having undergone ERCP with sphincterotomy for benign diseases between 1995 and 2015
Exclusion Criteria:
  • Diagnosis of primary malignant tumors in the liver, bile ducts including ampullary region, and pancreas in the ERCP test.

  • Patients with follow-up less than two years after the ERCP and biliopancreatic malignancy diagnostic in this period.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Juan Carlos Martín del Olmo

Investigators

  • Study Director: Juan Carlos Martin Del Olmo, MD, PhD, Hospital Medina del Campo
  • Principal Investigator: Mercedes Ibáñez García, MD, PhD, Hospital Medina del Campo
  • Study Chair: Carlos Guijarro, MD, PhD, Hospital Medina del Campo
  • Study Chair: Kostantin Shirai, MD, PhD, Hospital Medina del Campo
  • Study Chair: Cristina López Mestanza, MD, PhD, Hospital Medina del Campo

Study Documents (Full-Text)

More Information

Publications

Responsible Party:
Juan Carlos Martín del Olmo, MD, PhD. Associate Profesor Valladolid University, Hospital Medina del Campo
ClinicalTrials.gov Identifier:
NCT04735224
Other Study ID Numbers:
  • HMCampo2
First Posted:
Feb 3, 2021
Last Update Posted:
Feb 3, 2021
Last Verified:
Jan 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Keywords provided by Juan Carlos Martín del Olmo, MD, PhD. Associate Profesor Valladolid University, Hospital Medina del Campo
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 3, 2021