ClinicalTrials.Veeva

Menu

Comparison Between Two Analgesic Methods for Pain Relief Following Surgical Abortion

R

Rambam Health Care Campus

Status

Unknown

Conditions

Pain

Treatments

Drug: lornoxicam
Drug: Paracetamol

Study type

Interventional

Funder types

Other

Identifiers

NCT02025166
RMB343-13
RMB0343-13 (Other Identifier)

Details and patient eligibility

About

To compare between the efficacy of Paracetamol IV vs. Lornoxicam IV in pain relief following surgical abortion.

The medication will be given at the time of the procedure. Following the abortion, pain level will be evaluated.

Full description

Patients with medical indication for surgical abortion during first trimester will be divided to two groups. The study groups, the surgeons and the nurses will be blinded to one of the treatment arms.

Pain will be evaluated at fixed intervals following the abortion. Comparison in pain levels between the study groups will be analysed.

Enrollment

82 estimated patients

Sex

Female

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Elective surgical abortion for first trimester pregnancy

Exclusion criteria

  • Chronic pelvic pain
  • Fibromyalgia
  • Pelvic inflammatory disease
  • Chronic renal failure, liver disease, peptic ulcer
  • cervical stenosis

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

82 participants in 2 patient groups

Paracetamol
Active Comparator group
Description:
Pain treatment, aniline analgesics
Treatment:
Drug: Paracetamol
Drug: lornoxicam
lornoxicam
Active Comparator group
Description:
Pain treatment, nonsteroidal anti-inflammatory (NSAID)
Treatment:
Drug: Paracetamol
Drug: lornoxicam

Trial contacts and locations

1

Loading...

Central trial contact

Lior Lowenstein, MD, MS

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems