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Pre-emptive Paracetamol for Prevention of Intraoperative Shoulder Tip Pain

Cairo University (CU) logo

Cairo University (CU)

Status and phase

Unknown
Phase 3
Phase 2

Conditions

Cesarean Section

Treatments

Drug: Saline Solution
Drug: paracetamol

Study type

Interventional

Funder types

Other

Identifiers

NCT04038307
MS-12-2019

Details and patient eligibility

About

the aim is to determine the efficacy of Paracetamol in reducing the incidence and severity of intraoperative shoulder pain in patients undergoing cesarean section.

Full description

pregnant females scheduled for cesarean section under spinal anesthesia will be enrolled . two groups of patents will be recruited . the study group will receive paracetamol pre operative .

Enrollment

120 patients

Sex

Female

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Healthy pregnant women (ASA II) having singleton pregnancy at term (≤ 37 weeks of gestation) aged between 18 and 40 years.

Exclusion criteria

  • Patients having allergy to study drug,
  • gestational diabetes
  • cardiovascular or biliary disorders
  • asthma
  • renal impairment
  • preeclampsia
  • any chronic pain condition or trauma in the shoulder, forearms or upper limbs
  • patients with any contraindication to SA were excluded from the study.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

120 participants in 2 patient groups, including a placebo group

control
Placebo Comparator group
Description:
will receive 100 ml of saline
Treatment:
Drug: Saline Solution
paracetamol group
Experimental group
Description:
will receive 1gm paracetamol (100ml)
Treatment:
Drug: paracetamol

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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