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Clinical Trials/NCT04580329
NCT04580329UnknownNot Applicable

The Effect of Neuromuscular Electrical Stimulation (NMES) on the Renal Function and Renal Blood Flow for Patients With Pregnancy Related- Acute Kidney Injury

Ahmed talaat ahmed aly2 sites in 1 country60 target enrollmentStarted: October 15, 2020Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
60
Locations
2
Primary Endpoint
renal function change

Study Overview

Brief Summary

A randomized prospective controlled study aims to evaluate the effect of neuromuscular electrical stimulation on the renal function and renal blood flow of post partum women with acute kidney injury.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
18 Years to 60 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patients aged 18 or old and hemodynamically stable.
  • •Post-partum women who developed AKI.

Exclusion Criteria

  • •Pregnant women .
  • •Patients who required any emergency or elective surgery during the study; those who presented acute heart or lung disease, skin rashes, tumors, infections, diabetes mellitus or hypoesthesia in the region that the neuromuscular electrical stimulation would be applied.
  • •Patients with a Pacemaker.
  • •Epileptic Patients.
  • •Patients with recent effects of stroke (less than 3 months).
  • •Uncontrolled hypertension (systolic blood pressure > 230 mm Hg and diastolic blood pressure > 120 mm Hg).

Arms & Interventions

NMES group

Experimental

Intervention: neuromuscular electrical stimulation (NMES) in addition to routine hospital care (Procedure)

control group

Experimental

Intervention: routine hospital care without NMES (Procedure)

Outcomes

Primary Outcomes

renal function change

Time Frame: for 7 days

serum creatinine level will be assessed and it will show improvement

renal blood flow change

Time Frame: for 7 days

urine output will be assessed and it will show improvement

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Ahmed talaat ahmed aly
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Ahmed talaat ahmed aly

clinical professor

Assiut University

Study Sites (2)

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