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Study of Pain Control in Diagnostic Hysteroscopy

P

Phramongkutklao College of Medicine and Hospital

Status

Completed

Conditions

Pain, Postoperative

Treatments

Combination Product: Ibuprofen-Paracetamol

Study type

Interventional

Funder types

Other

Identifiers

NCT06188143
PMK-019

Details and patient eligibility

About

The goal of this clinical trial study is to learn about how to decrease the pain during the diagnostic hysteroscopy. The main question it aims to answer is "Do the Paracetamol and Ibuprofen taken before the procedure can lower the pain during the diagnostic hysteroscopy".

Full description

After the participants those are indicated for diagnostic hysteroscopy and eligible for the study undergo informed consent, then they were divided to two groups for control group those get no medication and study group those get Paracetamol 500mg and Ibuprofen40mg per oral before the hysteroscopy, and both group needs to evaluate the pain score in VAS before, during hysteroscopy and after hysteroscopy for 30 minutes to compare the pain level in two groups.

Enrollment

58 patients

Sex

Female

Ages

20+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Women with indication and informed to undergo diagnostic hysteroscopy over or equal the age of 20 years old

Exclusion criteria

  • Women with contraindication for undergoing diagnostic hysteroscopy includes women with pregnancy, uterine infection, diagnosed with cervical cancer or endometrium cancer and women who is undergoing with active vaginal bleeding
  • Women with history of allergy to Paracetamol or Ibuprofen medicine
  • Women with currently or pre-existing medical conditions that contraindicate the use of ibuprofen includes kidney disease, heart disease, cirrhosis, gastritis or individuals with a history of peptic ulcer or gastrointestinal bleeding
  • Women with currently taking anticoagulant or antiplatelet medications
  • Women with history of psychiatric disorders

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

58 participants in 2 patient groups

Control group
No Intervention group
Description:
No medication before hysteroscopic procedure
Ibuprofen-Paracetamol
Experimental group
Description:
Ibuprofen 40mg and Paracetamol 500mg per oral, single dose each, before hysteroscopic procedure 30minutes
Treatment:
Combination Product: Ibuprofen-Paracetamol

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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