caeserean section
Conditions
Interventions
Sponsors
DR. ATONGO TERNGU JESSE
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Patients who had caesarean delivery under spinal anesthesia that consented.
Exclusion criteria
Exclusion criteria: 1. Patients who had caesarean delivery under general anesthesia, epidural combined spinal 2. Patients with medical condition known to be potentially exacerbated by non-steroidal anti-inflammatory drugs such as peptic ulcer disease, renal .disease, Asthma liver disease 3. History of allergy to either of the study medications. 4. Patients with bleeding disorder. 5. Any patient who required special post-operative pain control such as sickle cell disease patient. 6. Patients who did not consent to the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1)To compare the effectiveness of intramuscular Pentazocine with rectal diclofenac sodium in post caesarean section pain relief. | — |
Secondary
| Measure | Time frame |
|---|---|
| 2) To compare maternal satisfaction with rectal diclofenac sodium and with intramuscular Pentazocine. ;To determine the side effects/adverse effects experienced by patients in the two groups | — |
Countries
Nigeria
Contacts
Public Contactwinifred Atongo
Analyst
Outcome results
None listed