Skip to main content
. 2009 Jul 8;2009(3):CD001548. doi: 10.1002/14651858.CD001548.pub2
Study Reason for exclusion
Ahlstrom 1989 No placebo control.
Akural 2009 Medication administered preoperativley.
Anaokar 1993 No placebo control.
Apaydin 1994 No placebo control.
Apiou 1988 No placebo control.
Aranda 1989 No placebo control.
Averbuch 2000 Not an original report of trials, and unable to ensure that participants (total of 75 treated with ibuprofen) were not in another included study.
Bailey 1993 No placebo control.
Behotas 1992 Baseline pain intensity was not moderate to severe.
Bhounsule 1990 Did not state whether patients had a baseline pain of at least moderate intensity.
Biehl 1981 No placebo control.
Bloomfield 1974 Used 5 point pain intensity scale which is not validated for the data extraction method.
Calanchini 1991 No placebo control.
Carlos 1984 Could not be obtained despite attempts to contact the authors, ordering through the British Library and help from the librarians at Novartis and Knoll pharmaceuticals.
Carrillo 1990 Did not state when the interventions were administered but as the pain levels were recorded for the first 4 hours following surgery it may be assumed that they were given immediately postoperatively. Therefore insufficient baseline pain.
Chopra 2009 Medication administered at 1 hour, irrespective of baseline pain.
Cooper 1984 Inadequate description of method. Did not state whether interventions were randomly allocated or studies were double‐blind.
Cooper 1988b Inadequate description of method. Did not state whether interventions were randomly allocated.
Cooper 1993 No placebo control.
Cooper 1996b Intervention administered irrespective of postoperative baseline pain.
Darsow 1988 No direct pain outcome measured over the first 4‐6 hours (recorded motility etc in the days following surgery).
Dorfmann 1991 Inadequate description of method. Did not say whether the allocation was randomised, did not say when the interventions were administered postoperatively, no mention of the level of baseline pain and did not define the pain measurement used.
Doyle 2002 No usable data for ibuprofen treatment arm.
El‐Tanany 1993 No placebo control.
Fleiss 1979 Take medication "if experience pain". Cannot assume that all the patients included had a baseline pain of >moderate intensity.
Forbes 1991 Used a controlled release formulation of ibuprofen.
Frezza 1985 Could not be obtained despite attempts to contact the authors, ordering through the British Library and help from the librarians at Novartis and Knoll pharmaceuticals.
Gallardo 1980 Baseline pain intensity not moderate to severe.
Gallardo 1981 Data was only collected for three hours.
Garwood 1983 No placebo control.
Giles 1981 No placebo control.
Giles 1985 Did not state which scale was used.
Hazra 1982 Baseline pain intensity not moderate to severe.
Henderson 1994 No placebo control.
Henrikson 1982 Only presented the data for the placebo arm for the first hour.
Henrikson 1985 No placebo control.
Hopkinson 1980 Five point pain intensity scale and 5 point pain relief scale (including "worse") neither of which are validated for the data extraction method used. Global evaluation was the opinion of the investigators rather than the patient.
Hultin 1978 Cross‐over study with the first dose administered exactly 1 hour after the local anaesthetic rather than when the patient experienced at least moderate pain.
Hyrkas 1992 Intervention administered preoperatively. Therefore inadequate baseline pain.
Hyrkas 1993 Intervention administered preoperatively. Therefore inadequate baseline pain.
Hyrkas 1994 Intervention administered preoperatively. Therefore inadequate baseline pain.
Iles 1980 Data was only presented for one hour after administration of the interventions.
Iqbal 1986 Could not be obtained despite attempts to contact the authors, ordering through the British Library and help from the librarians at Novartis and Knoll pharmaceuticals.
Iwabuchi 1980 No placebo control.
Joubert 1977 Could not be obtained despite attempts to contact the authors, ordering through the British Library and help from the librarians at Novartis and Knoll pharmaceuticals.
Katharia 1992 Multiple dose study with no separate analysis of the first dose.
Khan 1992 No placebo control.
Kittala 1972 Intervention routinely administered to all participants irrespective of level of baseline pain.
Klein 1994 Abstract.
Mastronardi 1988 No placebo control.
Matthews 1984 First dose was administered immediately postoperatively irrespective of patients level of pain.
McEvoy 1996 No placebo control.
McQuay 1993 No placebo control.
Movilia 1990 First dose was administered immediately postoperatively irrespective of patients level of pain.
Nakanishi 1990 No placebo control.
Negm 1989 Included participants who took the medication when they were experiencing only mild pain.
Rondeau 1980 Baseline pain intensity not moderate to severe.
Rossi 1981 Inadequate description of method. Did not state whether study was double blind. Also data was only recorded for three hours.
Schleier 2007 No placebo control.
Shimura 1981 No placebo control.
Squires 1981 Intervention administered preoperatively. Therefore inadequate baseline pain.
Tai 1992 No placebo control.
Tani 1974 No placebo control.
Tesseroli 1986 The only measure of pain which was in the opinion of the patient rather than the investigator was the pain intensity VAS. At baseline, the mean VAS minus 1.96 x SD was less than 30 mm, therefore some patients included may have had a baseline pain intensity of less than moderate.
Troullos 1990 Intervention administered preoperatively. Therefore inadequate baseline pain.
Turcotte 1986 Baseline pain intensity not moderate to severe.
Van Der Zwan 1982 No direct pain outcome measurement used, pain assessed by analgesic intake.
Van Wering 1972 No placebo control.
Vigneron 1977 Could not be obtained despite attempts to contact the authors, ordering through the British Library and help from the librarians at Novartis and Knoll pharmaceuticals.
Vogel 1984 Combined the data from separate arms of a cross‐over trial into one data set.
Von Mayer 1980 Multiple dose study with no mention of the level of baseline pain.
Walker 1976 No placebo control.
Walton 1990 Intervention administered preoperatively. Therefore inadequate baseline pain.
Walton 1993 First dose was given im during surgery, then oral doses were given postoperatively at specified times rather than when patients had baseline pain of at least moderate intensity.
Weber 1990 No placebo control.
Winter 1978 Baseline pain intensity not moderate to severe.
Wuolijoki 1987 Interventions were administered either pre‐operatively or immediately post‐operatively. Therefore insufficient baseline pain.