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Pain and Suction Curettage

NCT ID: NCT01947205

Last Updated: 2013-09-20

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

NA

Total Enrollment

111 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-11-30

Study Completion Date

2013-08-31

Brief Summary

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Aim of the study was to investigate the analgesic efficacy of preoperative oral dexketoprofen trometamol, intravenous paracetamol, lidocaine spray and paracervical block with ultracaine on curettage procedure.

Detailed Description

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Conditions

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Curettage Analgesia Paracervical Block Paracetamol

Keywords

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Curettage analgesia paracervical block paracetamol lidocaine Dexketoprofen trometamol

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

FACTORIAL

Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Caregivers Investigators

Study Groups

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paracetamol

Duration

Group Type ACTIVE_COMPARATOR

paracetamol

Intervention Type DRUG

without drug

Control group

Group Type ACTIVE_COMPARATOR

without drug

Intervention Type OTHER

dexketoprofen trometamol

Study group

Group Type ACTIVE_COMPARATOR

dexketoprofen trometamol

Intervention Type DRUG

two puff xylocain administration on cervical surface

Study group

Group Type ACTIVE_COMPARATOR

suction curettage

Intervention Type DRUG

paracervical block with ultracaine

study group

Group Type ACTIVE_COMPARATOR

suction curettage

Intervention Type DRUG

Interventions

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paracetamol

Intervention Type DRUG

dexketoprofen trometamol

Intervention Type DRUG

suction curettage

Intervention Type DRUG

suction curettage

Intervention Type DRUG

without drug

Intervention Type OTHER

Other Intervention Names

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two puff xylocain administration paracervical block with ultracaine

Eligibility Criteria

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Inclusion Criteria

* pregnant participants between 35-48 days of gestation (5 to 7 weeks of gestation) pregnant participants with a single viable intrauterine pregnancy requesting termination of pregnancy.

Exclusion Criteria

incomplete abortions, diabetes mellitus, tendency to bleed such as thrombocytopenia, factor deficiency and functional disorders of platelets… etc, pelvic infection, known cervical stenosis, significantly impaired respiratory or cardiac conduction functions, active liver disease, renal disease, previous adverse reaction to any of the drugs used in the study, and patients who are unable to understand how to score a 10-cm visual analog scale (VAS) pain score. Moreover, patients who described chronic pelvic pain prior to the study or patients who rated their pain level on a continuous 100-mm VAS different from 0 (no pain) just before the study were not included into study.
Minimum Eligible Age

16 Years

Maximum Eligible Age

45 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Gökhan Açmaz

OTHER_GOV

Sponsor Role lead

Responsible Party

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Gökhan Açmaz

Kayseri Education and Research Hospital

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Gökhan Açmaz, MD

Role: PRINCIPAL_INVESTIGATOR

Kayseri Education and Research Hospital

Locations

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Kayseri Education and Research Hospital of Medicine

Kayseri, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

References

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Acmaz G, Aksoy H, Ozoglu N, Aksoy U, Albayrak E. Effect of paracetamol, dexketoprofen trometamol, lidocaine spray, and paracervical block application for pain relief during suction termination of first-trimester pregnancy. Biomed Res Int. 2013;2013:869275. doi: 10.1155/2013/869275. Epub 2013 Dec 24.

Reference Type DERIVED
PMID: 24455735 (View on PubMed)

Other Identifiers

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KayseriERH

Identifier Type: OTHER

Identifier Source: secondary_id

Kayseri ERH

Identifier Type: -

Identifier Source: org_study_id