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Not yet recruitingNCT07170397Updated Aug 4, 2026

Effects of Laser Acupuncture Treatment in Hypertension Haemodialysis Patients

An interventional study of Acupuncture Laser Therapy in Hypertension, sponsored by Sinai University. Not yet recruiting at 2 sites in Egypt. Open to participants aged 18 Years to 60 Years. Per ClinicalTrials.gov, last updated 2026-08-04.

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

Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Not applicable
Ages
18 Years to 60 Years
Sex
All
01

Study summary

The purpose of this study is to find the effect of acupuncture laser therapy on Blood Pressure in Hypertension Haemodialysis Patients

Read the detailed description

In patients with end-stage renal disease (ESRD) receiving dialysis, elevated blood pressure is common and poorly controlled in general. Although volume overload and sodium retention appear to be the main pathogenic mechanism of hypertension in this population, other factors such as increased arterial stiffness, activation of renin-angiotensin-aldosterone system, sleep apnea, activation of sympathetic nervous system, and use of recombinant erythropoietin may be also involved. Acupuncture laser therapy, which uses low-level laser treatment at specific acupuncture points, has shown promise in reducing blood pressure without invasive procedures. However, its specific efficacy in hemodialysis patients remains underexplored, necessitating this research

02

Conditions studied

  • Hypertension

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Keywords

  • laser Acupuncture Treatment, Blood Pressure, Hypertension Haemodialysis Patients
03

In context

Hypertension

6,114 studies on the registry are indexed under Hypertension; 912 are open to participants now.

This study's planned enrollment of 60 is below the median of 100 across 4,575 interventional studies indexed under Hypertension.

Browse Hypertension studies →

Lead sponsor

Sinai University is the lead sponsor of 24 studies on the registry; 11 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • sixty hemodialysis patients undergoing physical therapy treatments will participate in the study. Their mean age will range from (18-65) years old

Exclusion criteria

Exclusion Criteria:

  • a failure to take part in more than three light therapy sessions; a kidney transplant; and death
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
60 participants (estimated)

Study arms

  • Active comparator
    Efficacy of of Acupuncture Laser Therapy on Hemodialysis

    Patients receive Acupuncture Laser Therapy

    Device: Acupuncture Laser Therapy

Interventions

  • DeviceAcupuncture Laser Therapy

    Application of low-level laser therapy to patients with chronic kidney disease to evaluate its effects on pain, circulation, and functional outcomes

06

What researchers measure

Primary outcomes

  1. Change in systolic and diastolic blood pressure

    Blood pressure will be measured using a calibrated sphygmomanometer

    Time frame: Baseline and after 4 weeks of low-level laser therapy

  2. Blood pressure

    Blood pressure will be measured using a calibrated sphygmomanometer

    Time frame: Baseline and after 4 weeks of low-level laser therapy

07

Study locations

2 sites
  • Cairo university- Faculity of physical therapy
    Cairo, Cairo Governorate 11562, Egypt
  • Sinai university- Faculity of physical therapy
    El Arish, Sinai 11562, Egypt
08

References and documents

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Aug 2026; primary completion for Oct 2027, 13 months later.

Of 1,403 non-industry interventional studies with no phase under Hypertension, half reached primary completion within 23 months of starting (the median), counting those still running; a quarter within 10 and three quarters within 41. This study's planned 13 months is below that.

Counting every sponsor, half of 1,498 studies reached it within 23 months; a quarter within 10 and three quarters within 41.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 5, 2025
First posted
Sep 12, 2025
StartEst.
Aug 3, 2026
Primary completionEst.
Oct 1, 2027
CompletionEst.
Dec 1, 2027
Last update
Aug 4, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 4, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07170397
Lead sponsor
Sinai University
Responsible party
Amany Gomaa Atiaa (Lecturer in Physical Therapy, Sinai University) — Principal investigator
First posted
Sep 12, 2025
Start date
Aug 3, 2026 (estimated)
Primary completion
Oct 1, 2027 (estimated)
Completion
Dec 1, 2027 (estimated)
Last update
Aug 4, 2026

Study contacts

Shimaa Galal Elsayed, lecturer
Contact
shimaagalal1986@gmail.com
+20-100-311-9152

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

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