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Laser Puncture and Program of Lifestyle Modification in Lupus Females

Laser Puncture and Program of Lifestyle Modification in Lupus Females: Lipid Profile Response

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05381545
Enrollment
64
Registered
2022-05-19
Start date
2022-02-28
Completion date
2022-07-01
Last updated
2022-05-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Systemic Lupus Erythematosus

Brief summary

Serum lipid profile was significantly dysregulated in female systemic lupus erythematosus (SLE) patients

Detailed description

the research will recruit 64 female systemic lupus erythematosus (SLE) obese patients to divide them to two study groups equally. the study groups will receive, for 12 weeks, energy expenditure program (Pilates exercise, managed 5 times per week, combined with low calorie diet for).One group only will receive an additional laser puncture (with 3-time per-week design). The following points will be directly contacted by laser, for two minutes: GB34&28, ST25&36&40, SP6, and CV4&9&12.

Interventions

BEHAVIORALlaser puncture, energy expenditure programming, and low-calories recommended diet programming

This research group will receive, for 12 weeks, energy expenditure program (Pilates exercise, managed 5 times per week) combined with low calorie diet .This research group will receive an additional laser puncture (with 3-time per-week design). The following points will be directly contacted by laser, for two minutes: GB34&28, ST25&36&40, SP6, and CV4&9&12.

BEHAVIORALenergy expenditure programming and low-calories recommended diet programming

This research group will receive, for 12 weeks, energy expenditure program (Pilates exercise, managed 5 times per week) combined with low calorie diet.

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* obese female participants * Lupus females

Exclusion criteria

* pregnant lupus female * lactating lupus females * neurologic or articular disorders * another autoimmune conditions

Design outcomes

Primary

MeasureTime frameDescription
triglycerides12 weeksa lipid component will be measured in blood of females

Secondary

MeasureTime frameDescription
high density lipoprotein12 weeksa lipid component will be measured in blood of females
cholesterol12 weeksa lipid component will be measured in blood of females
low density lipoprotein12 weeksa lipid component will be measured in blood of females

Countries

Egypt

Contacts

Primary ContactAli Ismail, lecturer
allooka2012@gmail.com02 01005154209

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026