Introduction Venlafaxine is a nontricyclic antidepressant that selectively inhibits serotonin reuptake at low doses, but at higher doses, it blocks neuronal reuptake of serotonin, norepinephrine, and, to a lesser degree, dopamine (Debonnel et al., 2007).
Venlafaxine was also proved to have analgesic and antinociceptive effects through opioid mechanisms (Markowitz \& Patrick, 1998; Schreiber et al., 1999; Schreiber et al., 2002).
In the study of McDowell et al. (2000), venlafaxine was successfully used to treat patients with cocaine dependence comorbid with major depression. In animal studies, venlafaxine demonstrated effectiveness to attenuate morphine withdrawal symptoms (Lu et al., 2001) and attenuate acquisition of intravenous self-administration of heroin in rats (Magalas et al., 2005). Lin et al. (2008) found that venlafaxine is effective in alleviating withdrawal symptoms of heroin with good tolerability and safety.
Lofixidine works by blocking the release of norepinephrine, a hormone similar to adrenaline that contributes to opioid withdrawal symptoms. Lofexidine is a non-opioid prescription medicine used in adults to help with the symptoms of opioid withdrawal that may happen when you stop taking an opioid suddenly.
Naltrexone, is an opioid antagonist, without abuse liability and the oral formulation was found to be a safe option for motivated individuals who prefer not to be treated with opioid agonist medication or where opioid agonist medications are not legally available (Krupitsky et al., 2010, Ling et al., 2012, Mooney, 2016). Although oral naltrexone had a limited side effect profile, the clinical evidence demonstrating its efficacy for the treatment of opioid use disorder has revealed limitations in its use, particularly as it requires detoxification and a several days period of opioid abstinence prior to initiation (Ling et al., 2012, Nunes et al., 2015, Mooney, 2016).
Rational Tramadol abuse is a public health problem in Egypt affecting both adults and adolescents. Dissatisfaction with current available regimens for treatment of tramadol abuse has led to the search for alternatives. This study will investigate the efficacy and tolerability of venlafaxine versus lofexidine for management of withdrawal symptoms of tramadol abuse and venlafaxine versus naltrexone in preventing relapse.
Research question:
* Is venlafaxine as effective as lofexidine for treatment of tramadol withdrawal symptoms?
* Is venlafaxine as effective as naltrexone in relapse prevention of tramadol abuse?
HYPOTHESIS:
We assume that venlafaxine is as effective as lofexidine for treatment of tramadol withdrawal symptoms and as effective as naltrexone in prevention of tramadol relapse.
AIM:
\- This study aims at finding an effective and safe treatment for patients with tramadol abuse.
OBJECTIVES:
1. To compare the efficacy of venlafaxine versus lofexidine for treatment of tramadol withdrawal symptoms.
2. To compare the efficacy of venlafaxine versus naltrexone in prevention of tramadol relapse.
SUBJECTS AND METHODS:
I -Technical design This study was be carried out at the outpatient clinics and inpatient wards of addiction unit at Zagazig university hospitals, Egypt.
Sample size Assuming that the mean number of opioid negative tests in a previous study comparing buprenorphine and naltrexone in relapse prevention was 19.7+\_6.1 for buprenorphine VS 15.4+\_4.9 for naltrexone. The sample was estimated to be 52 cases of tramadol abuse (26 cases in each treatment group) with 95% confidence interval and 80% test power (open epi program).
II-Operational design:
This was a a randomized comparative clinical trial, which included 52 patients with tramadol abuse who were divided randomly into 2 groups:
Detoxification stage (10 days) Group 1: patients received venlafaxine xr 75mg once daily + symptomatic treatment.
Group 2: received lofexidine .2mg ( 0.8 - 1.6 mg per day) + symptomatic treatment.
Relapse prevention stage (2 month) Group 1: patients continued to use venlafaxine xr, which increased gradually on weekly intervals to 225 mg/d Group 2: patients used naltrexone 50mg/d The diagnosis of tramadol abuse and any comorbid psychiatric disorder was based on the Structured Clinical Interview for DSM-IV axis I disorders (SCID-I) done on Day 1 of the study (First et al., 2012). The severity of withdrawal symptoms was assessed using the Clinical Opiate Withdrawal Scale (COWS) done on day 3 and 10 of the study (Wesson \& Ling, 2003). Hamilton anxiety rating scale (HAM-A) (Hamilton, 1959), Hamilton depression rating scale (HAM-D) (Hamilton, 1960) and Beck Depression Inventory (Beck et al., 1996) were used to assess anxiety and depressive symptoms on day 1 and at the end of the study after 2 months. Urine screen for drugs of abuse was done twice weekly to verify abstinence. Craving was assessed monthly. Outcome measures were treating tramadol withdrawal symptoms, the retention rate in every group and the result of urine screen test at the end of the study.
III-Administrative design:
1. Approval was obtained from the Institutional Review Board (IRB) and the Department of Psychiatry, Zagazig University, Egypt.
2. A written consent was signed by the study participants.
