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Aerobic Exercises on Persisted Post Burn Anemia

Cairo University (CU) logo

Cairo University (CU)

Status

Active, not recruiting

Conditions

Burns

Treatments

Procedure: Aerobic exercise and medical treatment
Dietary Supplement: Medical treatment group

Study type

Interventional

Funder types

Other

Identifiers

NCT06849479
P.T.Rec/012/005217

Details and patient eligibility

About

Fourty patients who have total body surface area ranged from 20% to 35% of burn, anemic and 8th to 16th week post burn will participate in this study, the patients will be randomly divided into two equal groups (20 patients for each group): Group A (Experimental Group) (Aerobic exercise and medical treatment):

Group B ( Control Group) (Medical treatment group):

Enrollment

40 patients

Sex

All

Ages

20 to 35 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

The subject selection will be according to the following criteria:

  1. Ages of patients will be ranged from 20 to 35 years.
  2. All patients underwent severe burn with TBSA ranged from 20% to 35%.
  3. 8 th to 16th week post burn.
  4. All patients will be referred with persisted anemia by a surgeon before starting the study procedure.
  5. All patients will enter the study having their informed consent

Exclusion criteria

The potential participants will be excluded if they meet one of the following criteria: 16

  1. Patients with persisted pre burn anemia associated with systematic chronic disease such as coronary artery disease or chronic kidney disease.
  2. Patients with pre burn persisted anemia associated with autoimmune disease such as Rheumatoid arthritis, Systemic lupus erythematosus ,Vasculitis, Sarcoidosis, Inflammatory bowel disease (IBD).
  3. Unevaluated cardiac arrhythmia, Chronic bronchitis, poorly controlled type 1 diabetes, Extreme morbid obesity, Extreme underweight body mass index less than 12, Poorly controlled hypertension, Poorly controlled seizure disorder, Poorly controlled hyperthyroidism, Orthopedic limitation as fracture, .

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

40 participants in 2 patient groups, including a placebo group

Group A
Experimental group
Description:
This group includes 20 patients who had severe burn with total body surface area ranged from 20% to 35%. These patients will receive aerobic exercises in addition to medical treatment of anemia.
Treatment:
Dietary Supplement: Medical treatment group
Procedure: Aerobic exercise and medical treatment
Group B
Placebo Comparator group
Description:
This group includes 20 patients who had severe burn with total body surface area ranged from 20 to 35%. These patients will receive a medical treatment of anemia.
Treatment:
Dietary Supplement: Medical treatment group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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