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Enhanced Recovery After Surgery for SPK Transplantation Recipients

S

Second Affiliated Hospital of Guangzhou Medical University

Status

Completed

Conditions

Diabetic Nephropathy
Perioperative/Postoperative Complications
Transplant Complication

Treatments

Procedure: Enhanced recovery for SPK recipients

Study type

Interventional

Funder types

Other

Identifiers

NCT06095544
2020-hs-67

Details and patient eligibility

About

108 patients underwent elective SPK surgery were randomly divided into ERAS group (E) and routine care group (T). The ERAS group was consisted of evidenced-based systematic optimization approaches, while the control group received routine care.

Full description

Primary results: the postoperative length of stay (LoS) and hospitalization costs; second results: post-operative analgesia score (NRS) , the incidence of post-operative nausea and vomiting (PONV) , urinary catheter removal time by 7 days , post-operative gastric tube indwelling time, the incidence of ambulation within 6 days . the dosage of dobutamine using , the dosage of norepinephrine using, and the total amount of fluid and urine volume . MAP and lactate level . Peak systolic velocity (PSV) and (resistance index) RI of grafts were checked between two groups.

Enrollment

90 patients

Sex

All

Ages

20 to 62 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Patients were aged 20-62 years
  2. Body mass index (BMI) of 18.5-32.9 kg/m2
  3. Voluntary participation for elective SPK surgery
  4. ERSD and DN patients waiting for SPK transplantation surgery.

Exclusion criteria

  1. History of allergy to narcotic drugs
  2. cardiopulmonary insufficiency
  3. congestive heart failure
  4. myasthenia gravis
  5. neurological disease
  6. mental illness
  7. severe liver dysfunction
  8. hyperkalaemia
  9. malignant hyperthermia
  10. unwilling to participate in the study for any reason, or had participated in another study within the 3 months

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

90 participants in 2 patient groups

ERAS group
Experimental group
Description:
ERAS group was consisted of evidenced-based systematic optimization approaches
Treatment:
Procedure: Enhanced recovery for SPK recipients
Traditional group
No Intervention group
Description:
The control group received routine care

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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