Optimizing Analgesia for Endometrial Biopsy

NCT ID: NCT06540599

Last Updated: 2024-08-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE4

Total Enrollment

197 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-09-01

Study Completion Date

2022-11-01

Brief Summary

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

Detailed Description

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Conditions

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Analgesia

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Patients using intrauterine lidocaine for analgesia

Group Type ACTIVE_COMPARATOR

Analgesic

Intervention Type DRUG

comparing the effectiveness of analgesics in endometrial biopsy

Patients using oral dexketoprofen for analgesia

Group Type ACTIVE_COMPARATOR

Analgesic

Intervention Type DRUG

comparing the effectiveness of analgesics in endometrial biopsy

Patients using cervical lidocaine spray for analgesia

Group Type ACTIVE_COMPARATOR

Analgesic

Intervention Type DRUG

comparing the effectiveness of analgesics in endometrial biopsy

Patients using paracervical block with prilocaine for analgesia

Group Type ACTIVE_COMPARATOR

Analgesic

Intervention Type DRUG

comparing the effectiveness of analgesics in endometrial biopsy

Interventions

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Analgesic

comparing the effectiveness of analgesics in endometrial biopsy

Intervention Type DRUG

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Gaziosmanpasa Research and Education Hospital

OTHER_GOV

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Gaziosmanpaşa Training and Research Hospital

Istanbul, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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GaziosmanpasaTREHes

Identifier Type: -

Identifier Source: org_study_id

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