Post operative pain management following Myomectomy
Conditions
Interventions
Suppository Rectal Diclofenac group
Sponsors
Dr Chiadikobi John Irechukwu
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Participants willingness to participate in the study
Exclusion criteria
Exclusion criteria: 1. Women that declined consent 2. Women with significant diseases like rectal disorders, peptic ulcer disease, hepatic,hematological and cardiovascular diseases.3. History of chronic pain 4. History of bleeding coagulopathies 5. Use of general anaesthesia 6. Adverse reaction or hypersensitivity to diclofenac or pentazocine
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome will be the pain score assessed using the visual analogue scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary outcome measures will be patients’ satisfaction which will be assessed after 24 hours of administration of the drugs, the need and frequency of rescue analgesia and maternal side effects | — |
Countries
Nigeria
Contacts
Public ContactGeorge Eleje
Consultant Obstetrician and Gynaecologist Department of Obstetrics and Gynaecology Nnamdi Azikiwe University Teaching Hospital Nnewi Nigeria
Outcome results
None listed