CClinicalTrials.gg
Status unknownNCT05163977PEAPPUpdated Dec 20, 2021

Pancreatico Enteric Anastomosis Post Pancreaticoduodenectomy

An interventional study of Blumgart Anastomosis and Cattell Warren Anastomosis in Cancer of Pancreas, sponsored by Cairo University. Status unknown at 1 site in Egypt. Per ClinicalTrials.gov, last updated 2021-12-20.

Sponsored by Cairo University · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Dec 2021), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
90
Allocation
Randomized
Sex
All
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Study summary

The aim of this study is to make a step for evaluation and presentation of a safe technique for pancreatico-jejunostomy that help in minimizing post-operative morbidity and mortality in pancreatic cancer patient by comparing Blumgart anastomosis with Cattell warren technique of anastomosis.

Read the detailed description

Study Design This study is a randomized prospective clinical trial. Methods of randomization: Randomized block design

The objective of the study was to evaluate the effect of Blumgart anastomosis versus Cattell Warren techniques for pancreatico-jejunostomy regarding

  • Surgical technique
  • Peri-operative outcome including

    1. Length of hospital stay
    2. Post-operative pancreatic fistula
    3. ICU admission and stay
    4. Operative time
    5. Other morbidity and mortality

Data collection:

All data will be collected for each group and will be divided into Patients' factors, intraoperative and postoperative factors. Patients' factors include patients' demographics, co-morbidities, neoadjuvant treatment, Pathology and Biliary drainage. Intra-operative factors include type of Pancreaticoduodenectomy (PD) (Whether classic or PPPD), Operative time in hours and estimated blood loss in ml, pancreatic duct and texture of pancreas. Post-operative factors include the short term post-operative course which will be divided into specific complications (pancreatic leakage, biliary leakage, delayed gastric emptying, 2ry hemorrhage, intra-abdominal collection, deep wound infection, Portal Vein (PV) - Superior Mesenteric Vein (SMV) thrombosis and general surgical complications.

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Conditions studied

  • Cancer of Pancreas

Keywords

  • cancer pancreas
  • pancreatico-jejunostomy
  • pancreatico-enteric anasomosis
  • pancreatic anastomosis
  • post-operative pancreatic fistula
  • pancreaticoduodenectomy
  • whipple's procedure
03

In context

Pancreatic Neoplasms

3,235 studies on the registry are indexed under Pancreatic Neoplasms; 899 are open to participants now.

This study's planned enrollment of 90 is above the median of 46 across 2,424 interventional studies indexed under Pancreatic Neoplasms.

Browse Pancreatic Neoplasms studies →

Lead sponsor

Cairo University is the lead sponsor of 4,780 studies on the registry; 1,427 are open to participants now.

Of its 36 completed or terminated interventional studies of FDA-regulated products, 5 (14%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Known Pancreatic head cancer diagnosed radiologically.
  • Operable and borderline pancreatic cancer.
  • Patients who will undergo upfront surgery and those who received neoadjuvant chemotherapy are included.

Exclusion criteria

Exclusion Criteria:

  • Metastatic patients.
  • Locally advanced cases.
  • Patients with comorbidities who are unfit for major surgical procedures.
  • Patients with very small pancreatic duct where the pancreatic duct can't be identified.
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
90 participants (estimated)

Study arms

  • Active comparator
    Cattell Warren Anastomosis

    Procedure: Cattell Warren Anastomosis

  • Experimental
    Blumgart Anastomosis

    Procedure: Blumgart Anastomosis

Interventions

  • ProcedureBlumgart Anastomosis

    The anti-mesenteric border of the jejunal loop proximal to the hepatico-jejunostomy is brought against the pancreatic stump. With the pancreatic stump retracted by the stay sutures, the transected end of pancreatic duct is first identified and secured by means of a blunt tipped probe. Each trans-pancreatic, suture was performed using a single Polydioxanone (PDS) 3 -0 blunt needle. We usually take 4 sutures, 2 on each side of the duct. The process is repeated in the same manner with the remaining sutures which are tightened at the end to approximate the jejunum loop to the stump. A small stab incision is then made at the anti-mesenteric border of the jejunum and a duct to mucosa anastomosis is constructed using an interrupted 5-0 Prolene. The process is completed by placing each of the retained needles through the seromuscular layer of the anterior jejunal wall and each knot is tied over the jejunal wall which is then warped over the cut end of the stump

  • ProcedureCattell Warren Anastomosis

    It is a two layer, interrupted, end to side pancreatico-jejunostomy. First an interrupted sutures between the posterior capsule and the seromuscular layer of the jejunum was constructed using PDS 3-0 , then a duct to mucosa interrupted sutures were taken using PDS 5-0 and finally interrupted sutures between the anterior capsule and the jejunum . The main difference here is that the sutures are taken in a conventional way which is tangential to the pancreatic capsule and parenchyma

06

What researchers measure

Primary outcomes

  1. Post-Operative Pancreatic Fistula

    We used the International Study Group of Pancreatic Fistula (ISGPF) definition which is any measurable pancreatic fluid output after postoperative day 3 (containing more than three times the normal serum amylase level; more than 300 IU/L) with clinical signs of an infection and/or necessitating a change in clinical management.

    Time frame: Up to 10 days after the operation

Secondary outcomes

  1. Biliary leakage

    Any biliary output via percutaneous drains after the first postoperative day, or detected at a re-laparotomy

    Time frame: Up to 10 days after the operation

  2. Post-Operative bleeding

    including early and late bleeding (1-3 weeks post-operative) According to ISGPF it is defined as any bleeding from the surgical site with a drop in hemoglobin concentration greater than 3 g/dL with peripheral circulatory impairment requiring medical, surgical, or radiological intervention.

    Time frame: 1-3 weeks

  3. Hospital Stay

    the post operative hospital stay

    Time frame: Immediate after surgery and until the discharge of the patient ,including the readmission within the first 30 days after the operation

  4. Operative Time

    Time of the surgical procedure in hours

    Time frame: During the operation

  5. primary or reactionary hemorrhage

    Bleeding that occurs during or in the first day after the operation

    Time frame: During the operation and within the first 24 hours after the operation

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Study locations

1 of 1 sites recruiting
  • The Egyptian National Cancer Institute
    Cairo, Egypt
    Recruiting
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 20, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05163977
Lead sponsor
Cairo University
Responsible party
Ehab Abdulkarim Abdulmaksoud (Assistant Lecturer of Surgical Oncology, Cairo University) — Principal investigator
First posted
Dec 20, 2021
Start date
Jun 12, 2021
Primary completion
Dec 2022 (estimated)
Completion
Dec 2022 (estimated)
Last update
Dec 20, 2021

Study contacts

Ehab A Abdulmaksoud, Master
Contact
ehab.a.abdelmaksoud@cu.edu.eg
01099192044 ext. 002
Haitham A Othman, MD
Contact
haitham.fekry@nci.cu.edu.eg
01005890222 ext. 002
Ehab A Abdulmaksoud, master
principal investigator · National Cancer Institute Cairo University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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