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Investigating the effect of visceral manual therapy in improving uterine blood supply and pregnancy outcomes in infertile women with the problem of increased resistance of uterine vessels

Not Applicable
Conditions
Infertility.
Female infertility of uterine origin
N97.2
Registration Number
IRCT20230206057338N2
Lead Sponsor
Tabriz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Female
Target Recruitment
33
Inclusion Criteria

Age between 20-40 years
Having at least two history of failed transfers
Having 2 grade A or B embryo for transfers
Having uterine artery resistance above 1.76

Exclusion Criteria

Having any of the cases of congenital anomaly of the uterus
Having fibroids or any intrauterine lesions
Having severe endometriosis
Having uterine myomas
Having uterine adenomyosis
Having ovarian cysts and antral follicles larger than 12 mm in size
having severe ovulation disorder including long-term oligoamenorrhea, premature ovarian failure, and hypothalamic amenorrhea
Having any internal diseases related to blood flow disorders such as diabetes and dyslipidemia, anorexia, smoking and alcohol consumption.
Having special diets such as vegetarianism
Having autoimmune disease
Having hypertension and coagulation disorders
Having intrauterine adhesions (Asherman's syndrome)
Having organic injuries
Having uterine dysplasia
Having mental illnesses
Having mental disorders
Having severe depression
Having contraindications for estrogen therapy
Having anemia
Having hyperthyroidism
Having heart disease
Having liver disease
Having kidney disease
Having others diseases that lead to decreased menstruation.
If the embryos are not Grade A or B after resuscitation, if the thickness of the endometrium is less than 6 mm on the day of transfer, or if they do not follow the prescribed treatment (such as a mistake in taking or omitting intervention or examination sessions) they are not included in the study.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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