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The Differences of Complications Between LPD(Laparoscopic Pancreaticoduodenectomy) and OPD(Open Pancreaticoduodenectomy)

To Investigate The Difference of Complications and Short-term Prognosis Between Laparoscopic and Open Pancreaticoduodenectomy in Patients With Pancreatic Cancer Based on a Special Disease Cohort Database

Status
Enrolling by invitation
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06685939
Acronym
TDCBLAP
Enrollment
220
Registered
2024-11-13
Start date
2020-01-01
Completion date
2025-07-31
Last updated
2024-11-13

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

Conditions

Pancreatic Neoplasms

Keywords

pancreatic cancer, LPD, OPD, complication

Brief summary

Main objective: This project intends to design a simulated RCT project and clinically relevant RCT study to target, selecting the study titled Short-Term outcomes Following Laparoscopic vs Open Pancreaticoduodenectomy in Patients With Pancreatic Ductal Adenocarcinoma: A Randomized Clinical Trial (Short-term Outcomes of Laparoscopic versus Open Pancreaticoduodenectomy in Patients with Pancreatic Ductal Adenocarcinoma), use the cases in the Pancreatic Cancer Special Disease Cohort Database, compare the differences in complications and short-term prognosis between patients with pancreatic cancer after laparoscopic and open pancreaticoduodenectomy, investigate the efficacy and safety of laparoscopic pancreaticoduodenectomy, and provide the basis and reference of real-world data for clinical relevant studies. Secondary objective: To predict the incidence of postoperative complications and short-term outcomes of pancreatic cancer patients by comparing the difference of complications and short-term prognosis between laparoscopic and open pancreaticoduodenectomy, and to improve the treatment power of patients scheduled for surgery and postoperative patients.

Interventions

PROCEDURELPD

The patients who received the LPD

Sponsors

Ruijin Hospital
CollaboratorOTHER
Zhijun Bao
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age: 18 years old, with no gender limit; * Histologically confirmed or clinically diagnosed as pancreatic cancer by MDT (multidisciplinary team), without histopathological evidence; * Patients may receive LPD or OPD according to the MDT evaluation; * Patients understand and are willing to comply with the trial; * Signed written informed consent before patient enrollment; * Patients who meet the clinical guidelines for intent to treat. * Those who met each of the above criteria were included in the study.

Exclusion criteria

* Patients with distant metastasis found before or during surgery, including peritoneal, liver, distant lymph node metastasis, and other organ involvement; * Patients who need pancreatic neck or pancreatic tail, total pancreatic resection or other palliative surgery; * Preoperative anesthesia ASA score of 4 points; * A history of other malignant tumors; * Pregnant or lactating women; * Patients with severe mental disorders; * MDT evaluates patients with vascular invasion and requiring vascular resection based on abdominal imaging data; * Patients who have participated in other clinical trials within 3 months. Those who meet any of the above criteria were not included in the study.

Design outcomes

Primary

MeasureTime frameDescription
Overall survivefrom the day after surgery to 3 years
complicationduring the days Postoperative up to 1 yearany possible symptoms caused by surgery

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026