abnormal uterine bleeding
Conditions
Interventions
spinal anaethesia
Sponsors
faculity of medicine Suez canal university
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1-Age from 25-60 years with abnormal uterine bleeding 2- Patients with ultrasound findings of endometrial or cervical pathology which will require cervical and endometrial sampling. 3-Patients who were ASAI (American Society of Anesthesiologists') physical status Grade I, ASA II (ASA Grade II). 4-Controlled clinical illness as DM and hypertension. 5-No history of allergic reaction to the anaesthetic agents.
Exclusion criteria
Exclusion criteria: 1-Patients with mental or behavioral disorders that will impair or interfere with perioperative and follow-up procedures, 2-Bleeding tendency, 3- patients with cervicitis or pelvic inflammatory disease before treatment. 4-A known sensitivity to used drugs, 5-Pregnancy, 6-vaginismus
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare between paracervical block in pain control in dilation and curettage and the spinal anesthesia in women with abnormal uterine bleeding. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1- To determine the severity of the pain perceived by the patient in paracervical block anaethesia versus the spinal anesthesia in women with abnormal uterine bleeding. 2- To assess the complications associated with both procedures. 3- To obtain cervical and endometrial specimens from women with abnormal uterine bleeding for histopathological evaluation. | — |
Countries
Egypt
Contacts
Public Contactmagy refaat
professor of obstetrics and gynecology faculity of medicine suez canal university
Outcome results
None listed