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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05258552
Other study ID # enema for PD
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date February 2022
Est. completion date December 2024

Study information

Verified date February 2022
Source Air Force Military Medical University, China
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A prospective, randomized, controlled study was conducted to identify patients with end-stage renal disease who required open peritoneal dialysis catheterization, preoperative enema or no enema was used to evaluate the efficacy and safety of reducing catheter dysfunction.


Description:

A prospective, randomized, controlled study was conducted to identify patients with end-stage renal disease who required open peritoneal dialysis catheterization, preoperative enema or no enema was used to evaluate the efficacy and safety of reducing catheter dysfunction. All the patients were divided into two groups: preoperative enema group and no intervention group. The peritoneal dialysis malfuction were observed.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 136
Est. completion date December 2024
Est. primary completion date June 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age =18; - Maintenance peritoneal dialysis treatment is required for end-stage Renal Disease; - First-time open surgeon peritoneal dialysis catheterization patient; - Only straight double-cuff Tenckhoff dialysis catheters were used. - Willing to participate in this study and sign informed consent form. Exclusion Criteria: - peritoneal dialysis contraindication; - Enema contraindication; - Patients refuse enema; - Expected survival time < 3 months; - Catharsis such as Senna Leaf and lactulose used before operation or colonic dialysis and enema used 3 days before operation.

Study Design


Related Conditions & MeSH terms

  • Peritoneal Dialysis Access Failure

Intervention

Procedure:
enema
preoperative enema

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Air Force Military Medical University, China

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of Catheter dysfunction requiring intervention within 3 months of peritoneal dialysis catheterization 3 months
Primary Time of first peritoneal dialysis catheter dysfunction 6 months
Secondary Incidence of Catheter dysfunction requiring intervention within 6 months of peritoneal dialysis catheterization 6 months
Secondary Catheter survival time 6 months
Secondary Incidence of peritoneal dialysis-associated Peritonitis 6 months
See also
  Status Clinical Trial Phase
Not yet recruiting NCT04034628 - Improving the Outcomes of Peritoneal Dialysis (PD) Catheter Insertion