
Fig. 1.
Study flowchart in accordance with CONSORT 2025. G: gabapentin, C: control, T: trospium, CONSORT: consolidated standards of reporting trials.
Table 1.
Patients' demographic data and clinical characteristics
| Variables | Group G (N=40) | Group T (N=40) | Group C (N=40) | Used test value | P value | |
|---|---|---|---|---|---|---|
| Age in years | M ± SD | 51.98 ± 6.59 | 51.47 ± 8.29 | 50.38 ± 8.98 | 0.413* | 0.663 |
| Range | 40 – 64 | 40 – 65 | 25.7 – 69.81 | |||
| Males/Females | 31/9 | 32/8 | 30/10 | 0.287† | 0.866 | |
| BMI (kg.m−2) | M ± SD | 25.2 ± 3.76 | 26.82 ± 3.8 | 26.13 ± 4.01 | 1.789† | 0.172 |
| Range | 20 – 32 | 20 – 32 | 16.44 – 34.31 | |||
| ASA classification | I | 16 (40.0%) | 17 (42.5%) | 18 (45.0%) | 0.569† | 0.966 |
| II | 18 (45.0%) | 16 (40.0%) | 17 (42.5%) | |||
| III | 6 (15.0%) | 7 (17.5%) | 5 (12.5%) |
Table 2.
Causes of postoperative care in the intensive care unit and sites of spine surgery and their number (%)
| Causes of POC in the S-ICU | Group G (N=40) | Group T (N=40) | Group C (N=40) | Used test value | P value |
|---|---|---|---|---|---|
| Medical causes | 34 (85.0%) | 36 (90.0%) | 35 (87.5%) | 0.739* | 0.946 |
| Surgical causes | 4 (10.0%) | 3 (7.5%) | 4 (10.0%) | ||
| Anaesthesia-related causes | 2 (5.0%) | 1 (2.5%) | 1 (2.5%) | ||
| Spine surgery site | |||||
| Cervical | 7 (17.5%) | 6 (15%) | 5 (12.5%) | 1.583* | 0.812 |
| Dorsal | 3 (7.5%) | 2 (5%) | 1 (2.5%) | ||
| Lumbar | 30 (75%) | 32 (80%) | 34 (85.0%) | ||

Fig. 2.
The incidence of CRBD at 1, 2, 6, 12, and 24 hours after the study drugs administration. CRBD: catheter-related bladder discomfort, G: gabapentin, T: trospium, C: control.

Fig. 3.
The severity of CRBD at 1 hour after the study drugs administration. CRBD: catheter-related bladder discomfort, G: gabapentin, T: trospium, C: control.

Fig. 4.
The severity of CRBD at 2 hours after the study drugs administration. CRBD: catheter-related bladder discomfort, G: gabapentin, T: trospium, C: control.
Table 3.
Incidence and severity of catheter-related bladder discomfort at 1, 2, 6, 12, and 24 hours after intake of the study drugs
| CRBD incidence in hours | Group G (N=40) | Group T (N=40) | Group C (N=40) | Used test value | P value | |
|---|---|---|---|---|---|---|
| At 1 hour | 14 (35.0%) | 11 (27.5%) | 24 (60.0%) | 9.589* | 0.008† | |
| At 2 hours | 12 (30.0%) | 9 (22.5%) | 22 (55.0%) | 10.076* | 0.006† | |
| At 6 hours | 11 (27.5%) | 8 (20.0%) | 19 (47.5%) | 7.471* | 0.024† | |
| At 12 hours | 6 (15.0%) | 3 (7.5%) | 15 (37.5%) | 12.188* | 0.002† | |
| At 24 hours | 4 (10.0%) | 2 (5.0%) | 10 (25.0%) | 7.500* | 0.024† | |
| CRBD severity in hours | ||||||
| At 1 hour | Mild | 8 (57.1%) | 7 (63.6%) | 4 (16.7%) | 18.393* | 0.001† |
| Moderate | 5 (35.7%) | 4 (36.4%) | 6 (25.0%) | |||
| Severe | 1 (7.1%) | 0 (0.0%) | 14 (58.3%) | |||
| At 2 hours | Mild | 8 (66.7%) | 6 (66.7%) | 6 (27.3%) | 16.004* | 0.003† |
| Moderate | 4 (33.3%) | 3 (33.3%) | 4 (18.2%) | |||
| Severe | 0 (0.0%) | 0 (0.0%) | 12 (54.5%) | |||
| At 6 hours | Mild | 8 (72.7%) | 6 (75.0%) | 7 (36.8%) | 9.347* | 0.053 |
| Moderate | 3 (27.3%) | 2 (25.0%) | 5 (26.3%) | |||
| Severe | 0 (0.0%) | 0 (0.0%) | 7 (36.8%) | |||
| At 12 hours | Mild | 4 (66.7%) | 2 (66.7%) | 8 (53.3%) | 1.371* | 0.849 |
| Moderate | 2 (33.3%) | 1 (33.3%) | 5 (33.3%) | |||
| Severe | 0 (0.0%) | 0 (0.0%) | 2 (13.3%) | |||
| At 24 hours | Mild | 3 (75.0%) | 2 (100.0%) | 7 (70.0%) | 1.267* | 0.867 |
| Moderate | 1 (25.0%) | 0 (0.0%) | 2 (20.0%) | |||
| Severe | 0 (0.0%) | 0 (0.0%) | 1 (10.0%) | |||

Fig. 5.
Visual analogue pain scale (VAS) at 1, 2, 6, 12, and 24 hours after the study drugs administration. G: gabapentin, T: trospium, C: control.

Fig. 6.
Fentanyl total requirements in the first 24 hours after the study drugs administration in micrograms (µg) in 24 hours. G: gabapentin, T: trospium, C: control.
Table 4.
Visual analogue pain scale (VAS) at 1, 2, 6, 12, and 24 hours after the study drug administration and the total fentanyl requirements (µg) in 24 hours
| Timed VAS | Group G (N=40) | Group T (N=40) | Group C (N=40) | Used test value | P value | |
|---|---|---|---|---|---|---|
| At 1 hour | Median | 2 (1 – 4) | 2 (1 – 4) | 2 (1 – 4) | 0.123* | 0.941 |
| Range | 0 – 6 | 0 – 6 | 0 – 6 | |||
| At 2 hours | Median | 2 (1 – 3) | 2 (1 – 4) | 2 (1 – 4) | 0.212* | 0.900 |
| Range | 0 – 5 | 0 – 5 | 0 – 6 | |||
| At 6 hours | Median | 1 (0 – 2)† | 2 (1 – 2)‡ | 2 (1 – 2)‡ | 11.489* | 0.003§ |
| Range | 0 – 3 | 0 – 3 | 0 – 3 | |||
| At 12 hours | Median | 1 (0 – 1)† | 2 (0 – 2) ‡ | 2 (1 – 2)‡ | 8.536* | 0.014§ |
| Range | 0 – 3 | 0 – 3 | 0 – 3 | |||
| At 24 hours | Median | 1 (0 – 1) | 2 (0 – 2) | 2 (0 – 2) | 5.560* | 0.062 |
| Range | 0 – 3 | 0 – 3 | 0 – 3 | |||
| Total fentanyl doses (µg) | ||||||
| Mean ± SD | 850.08 ± 122.63† | 1437.03 ± 103.67‡ | 1425.58 ± 88.88‡ | 401.281¶ | < 0.001§ | |
| Range | 654 – 1025 | 1275 – 1661 | 1275 – 1661 | |||
Table 5.
Side effects of the study drugs
| Drugs’ side effects | Group G (N=40) | Group T (N=40) | Group C (N=40) | Used test value | P value | |
|---|---|---|---|---|---|---|
| Nausea/vomiting | 1 (2.5%) | 0 (0.0%) | 0 (0.0%) | 2.017* | 0.365 | |
| Facial flushing | 0 (0.0%) | 1 (2.5%) | 0 (0.0%) | 2.017* | 0.365 | |
| Dry mouth | 2 (5.0%) | 4 (10.0%) | 1 (2.5%) | 2.124* | 0.346 | |
| Headache | 0 (0.0%) | 1 (2.5%) | 0 (0.0%) | 2.017* | 0.365 | |
| Light headiness | 1 (2.5%) | 1 (2.5%) | 0 (0.0%) | 1.017* | 0.601 | |
| Constipation | 1 (2.5%) | 3 (7.5%) | 1 (2.5%) | 1.670* | 0.434 | |
| Agitation | 0 (0.0%) | 0 (0.0%) | 1 (2.5%) | 2.017* | 0.365 | |
| Ramsay sedation score | M ± SD | 2.38 ± 0.67 | 2.23 ± 0.73 | 2.08 ± 0.69 | 1.843† | 0.163 |
| Range | 1 – 3 | 1 – 3 | 1 – 3 |