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Postoperative Pain After Medical Abortion Under Local Anesthesia : Comparison of Several Analgesic Regimen

Postoperative Pain After Medical Abortion Under Local Anesthesia : a Prospective and Randomized Trial Comparing Several Analgesic Regimen

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00188071
Enrollment
240
Registered
2005-09-16
Start date
2002-09-30
Completion date
2003-08-31
Last updated
2017-11-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Abortion, Induced

Keywords

medical abortion, analgesia

Brief summary

* To compare postoperative analgesia by paracetamol 1gr or ketoprofen 100 mg or the combination of these two analgesics * each treatment beeing allocated by randomization

Detailed description

* 240 pregnant women who undewent a medical abortion by aspiration, under local anesthesia, (day case surgery) were enrolled after informed consent and signed approval * according to randomization, they received one hour before medical abortion procedure performed under local anesthesia of the cervix, one of these three diffrente analgesics : * paracetamol 1 gr * ketoprofen 100 mg * the association of both Postprocedure pain was recorded, by nurse, using a visual analog scale (VAS), 7 times before and after the procedure, until the discharge of the patient. * if VAS was above 40 on two consecutive measurements a morphine injection was given. * the number and total amount of morphine was recorded. * satisfaction was recorded within the 3 postoperative day by a telephone inquiry.

Interventions

DRUGparacetamol
DRUGketoprofen
DRUGketoprofen + paracetamol

Sponsors

University Hospital, Angers
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* pregnant women * medical abortion performed in day case surgery under local anesthesia * informed written consent

Exclusion criteria

* under 18 year old

Design outcomes

Primary

MeasureTime frame
postoperative pain rating

Secondary

MeasureTime frame
morphine consumption
patient satisfaction

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026