Pain and Nausea After Gallbladder Surgery

NCT ID: NCT06083558

Last Updated: 2023-10-16

Basic Information

• Recruitment Status: RECRUITING
• Total Enrollment: 50000 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2016-01-01
• Study Completion Date: 2028-03-31

Brief Summary

The study is primarily an exploratory study of quality registry data for a swedish national cohort of patients who have undergone gallbladder surgery or ERCP, with the aim of investigating the occurrence of pain and PONV (Postoperative Nausea and Vomiting) after gallbladder surgery. Furthermore, the investigators will explorer if there are factors related to the patient or the surgical procedure that are associated with a higher risk of PONV or pain.

Detailed Description

The project is a registry study with linked data from the Swedish national registry for gallbladder surgery (Gallriks) and the Swedish Perioperative Register (SPOR).

In SPOR, multiple variables are recorded and the main categories include patient characteristics, process data (e.g., times, operating room, planning, cancellations), surgical data (diagnosis, procedure, anesthesia type, times, deviations), and postoperative data (e.g., pain, nausea, complications, times, postoperative care level). The main variables of interest in this project are postoperative nausea and vomiting (PONV) and pain. In SPOR, it is possible to register whether the patient experienced nausea or vomiting and to assess pain in the immediate postoperative period during the stay at the postoperative recovery unit (PACU). The mean time of stay at PACU after gallbladder surgery in Sweden is 3.5 hours.

Gallriks records data related to gallstone surgery, including preoperative factors (including patient's illness), surgical processes, and postoperative outcomes up to 6 months after surgery.

The investigators have estimated that it is possible to include at least 50% of all gallstone surgeries in Sweden, which corresponds to a range of 7,000-8,000 patients per year.

Both quality registers are housed at the Uppsala Clinical Research Center (UCR), which will perform the data linkage. The data extraction process will start with the surgical cases in Gallriks and match them with SPOR. The database delivered to the research group will contain only pseudonymized personal data, with personal identification numbers and names removed.

The objectives of the study are:

• Describe the risk of early PONV (Postoperative Nausea and Vomiting) and pain during the PACU stay following gallstone surgery.
• Identify factors associated with early PONV and pain.
• Test the hypothesis that total intravenous anesthesia has a lower risk of PONV and pain at the PACU compared to inhalation-based anesthesia.
• Test the hypothesis that the addition of a regional block reduces the risk of PONV and pain during the PACU stay.
• Test the hypothesis that patients who experience PONV and/or pain in the postoperative ward have a higher risk of postoperative complications up to 6 months after surgery.

The primary outcome measures are:

• Risk of PONV in the postoperative ward (number of surgical cases with nausea and/or vomiting) / [total number of surgical cases].
• Median pain score (NRS) in the postoperative ward.
• Risk of severe pain (NRS>=7) [number of surgical cases with NRS>=7] / [total number of surgical cases].
• Percentage of patients with complications, unplanned hospitalizations, or reoperations after 30 days and 6 months.
• Based on the data in SPOR and Gallriks, identify factors associated with the primary outcome measures. Variables hypothesized to be associated include gender, age, illness, preoperative pain, type of anesthesia, type of surgery, and length of hospital stay.
• Specifically examine whether total intravenous anesthesia or regional blockade reduces the risk of PONV/pain and whether PONV/pain increases the risk of postoperative complications.

The data will be described using descriptive methods, and associations will be analyzed through univariate and multivariate analysis.

The study database is planned to include the procedures performed during the years 2016-2025. Databases will be delivered on a yearly basis. Analysis and reports/manuscripts from the study might include parts of the whole study period of 10 years.

Conditions

PONV; Postoperative Pain; Postoperative Complications; Gall Bladder Disease

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: OTHER

Eligibility Criteria

Inclusion Criteria

• Primary gallstone surgery
• Adult patients (>=18 years)
• Procedure performed between 2016 and 2025
• Surgical procedure registered in the national quality registry Gallriks.

Exclusion Criteria

• If multiple surgeries on the same patient in the study database, subsequent procedures to the first procedure is excluded.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Karolinska Institutet

OTHER

Sponsor Role: collaborator

Umeå University

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Jakob Wallden, MD PhD

Role: PRINCIPAL_INVESTIGATOR

Umeå University

Locations

Umeå University, Dept of surgical and perioperative sciences

Sundsvall, X, Sweden

Site Status: RECRUITING

Countries

Sweden

Central Contacts

Jakob Wallden, MD PhD

Role: CONTACT

jakob.wallden@umu.se

+46703644392

Tomi Myrberg, MD PhD

Role: CONTACT

tomi.myrberg@umu.se

Facility Contacts

Jakob Wallden, PhD MD

Role: primary

jakob.wallden@gmail.com

0703644392

Tomi Myrberg, PhD MD

Role: backup

tomi.myrberg@umu.se

Other Identifiers

GALLSPOR

Identifier Type: -

Identifier Source: org_study_id