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A randomized, double blind, and controlled clinical trial of the non-addictive propacetamol in postoperative analgesia / 中国医学科学院学报
Acta Academiae Medicinae Sinicae ; (6): 329-332, 2003.
Article in Chinese | WPRIM | ID: wpr-350098
ABSTRACT
<p><b>OBJECTIVE</b>To compare the postoperative analgesic efficacy and safety of the non-addictive propacetamol hydrochloride (Pro-Bufferin) injection and dolantin in a prospective, randomized, double blind and controlled clinical trial.</p><p><b>METHODS</b>After the pain intensity was assessed when the patients were undergone thoracic and abdominal selective surgery became fully conscious, 40 consecutive patients with moderate to severe postoperative pain (equivalent to Pain Grade I and II of American Anesthesia Association classification) were randomized into the study against the control groups. The two groups were similar for age, sex, height/weight, disease categories, operation categories, anesthesia methods and duration, vital signs, hepatorenal function, and blood cell count (P = 0.06-0.93). In the study group, 2 g propacetamol in 100 ml normal saline (NS) intravenously with 1.0 ml NS intramuscularly as the placebo control to dolantin were administered. In the control group, 1.6 g mannitose in 100 ml NS intravenously as the placebo control to propacetamol with 50 mg dolantin (1.0 ml) intramuscularly as the positive control to propacetamol were administered. The intensity change of postoperative pain was then evaluated 10 times with visual analog scale and verbal describing scale during 6 h from the beginning of propacetamol infusion. Vital signs and adverse reactions were also documented. After all data were put into the computer, the blinding codes were decoded and the statistic analysis was then made.</p><p><b>RESULTS</b>There was no significant difference (P = 0.93) about the area under the curve of "Pain Relieve Score vs. Time". The "starting to effect" time (15-30 min), analgesic duration (6 h) and the percentage of excellent or good analgesic effect (90%) in the two groups were the same. Adverse reactions didn't reached the statistic different level (P = 0.35).</p><p><b>CONCLUSIONS</b>Propacetamol HCL injection 2 g intravenously could be an alternative to dolantin 50 mg intramuscularly for moderate to severe postoperative pain with its advantage of being non-addictive.</p>
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pain, Postoperative / Double-Blind Method / Therapeutic Uses / Drug Therapy / Analgesics / Acetaminophen / Meperidine Type of study: Controlled clinical trial / Prognostic study Limits: Adult / Aged / Female / Humans / Male Language: Chinese Journal: Acta Academiae Medicinae Sinicae Year: 2003 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pain, Postoperative / Double-Blind Method / Therapeutic Uses / Drug Therapy / Analgesics / Acetaminophen / Meperidine Type of study: Controlled clinical trial / Prognostic study Limits: Adult / Aged / Female / Humans / Male Language: Chinese Journal: Acta Academiae Medicinae Sinicae Year: 2003 Type: Article