Optimizing Analgesia for Endometrial Biopsy

Gaziosmanpasa Research and Education Hospital

Status and phase: Completed; Phase 4

Conditions: Analgesia

Treatments: Drug: Analgesic

Study type: Interventional

Funder types: Other

Identifiers

NCT06540599

GaziosmanpasaTREHes

Details and patient eligibility

About

Comparison of the effectiveness of intrauterine lidocaine-paracervical block-dexketoprofen tromematol- lidocaine spray in endometrial biopsy analgesia

Enrollment: 197 patients

Sex: Female

Ages: 18 to 75 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• women aged 18-75 needs endometrial biopsy

Exclusion criteria

• women with allergies to prilocaine, lidocaine or dexketoprofen trometamol
• women with a history of severe uncontrolled cardiovascular disease, diabetes mellitus, pregnancy, vaginal, cervical, or pelvic infection, cervical cancer, or severe cervical stenosis

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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197 participants in 4 patient groups

Patients using intrauterine lidocaine for analgesia

Active Comparator group

Treatment:

Drug: Analgesic

Patients using oral dexketoprofen for analgesia

Active Comparator group

Treatment:

Drug: Analgesic

Patients using cervical lidocaine spray for analgesia

Active Comparator group

Treatment:

Drug: Analgesic

Patients using paracervical block with prilocaine for analgesia

Active Comparator group

Treatment:

Drug: Analgesic