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The study aim to study to evaluate whether IV paracetamol reduces morphine use after TAH. Primary objective was to compare postoperative morphine consumption between the IV paracetamol and control groups.
and Secondary objective was to compare postoperative pain scores using the Numeric Rating Scale OR NRS
We conducted a randomized, double-blind, placebo-controlled trial at our hospital (QSMH) , including women undergoing elective TAH The trial was conducted between October 2024 (two thousand twenty-four) and May 2025 (two thousand twenty-five) , with approval from the institutional review board.
Participants were randomized 1:1 (one to one) to receive IV paracetamol 1 g or IV normal saline, administered in the operating room before induction of anesthesia, Postoperatively, pain was assessed intermittently using the NRS (āšnumeric rating scale) at 1, 6, 12, and 24 hours, with morphine 0.1 mg/kg (zero point one milligrams per kilogram) Intravenous provided on demand.
The primary outcome was the number of morphine injections within 24 hours; the secondary outcome was NRS pain scores.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Paracetamol | Experimental | Patients which recieved intravenous paracetamol preoperatively |
|
| Placebo | Placebo Comparator | Patients which recieved placebo preoperatively |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Paracetamol | Drug | Patients receive IV paracetamol 1 gm Postoperatively morphine 0.1 mg/kg was given intravenous provided on demand at at 1, 6, 12, and 24 hours. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Compare postoperative morphine consumption between the IV paracetamol and control groups. | at 1, 6, 12, and 24 hours postoperation |
| Measure | Description | Time Frame |
|---|---|---|
| Compare postoperative pain scores using the Numeric Rating Scale OR NRS | at 1, 6, 12, and 24 hours postoperation |
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Inclusion criteria
Exclusion criteria
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| Name | Affiliation | Role |
|---|---|---|
| Panumat Phungtippimanchai | Queen Savang Vadhana Memorial Hospital, Thailand | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Queen Savang Vadhana Memorial Hospital, Thai Red Cross Society, Jermjomphon street, Chonburi, 20110, | Chon Buri | Thailand |
data was save in form of microsoft excel spreadsheet and SPSS file
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| ID | Term |
|---|---|
| D010149 | Pain, Postoperative |
| ID | Term |
|---|---|
| D011183 | Postoperative Complications |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D010146 | Pain |
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| ID | Term |
|---|---|
| D000082 | Acetaminophen |
| ID | Term |
|---|---|
| D000083 | Acetanilides |
| D000813 | Anilides |
| D000577 | Amides |
| D009930 | Organic Chemicals |
| D000814 |
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| Placebo | Drug | Pateint recieved IV normal saline Postoperatively, pain was assessed intermittently using the NRS (āšnumeric rating scale) at 1, 6, 12, and 24 hours |
|
| D009461 | Neurologic Manifestations |
| D012816 | Signs and Symptoms |
| Aniline Compounds |
| D000588 | Amines |